diff --git a/Changelog.md b/Changelog.md
--- a/Changelog.md
+++ b/Changelog.md
@@ -21,3 +21,5 @@
 V 1.3.0: Removed pipes-text, text and turtle dependencies and some more. Restructured all datatypes to use Bytestring instead of text. 
 
 V 1.3.1: Moved test suite outside of the main library into the test source directory. Cleaner setup.
+
+V 1.3.2: Added testDat to Cabal file to make tests work off the tarball.
diff --git a/sequence-formats.cabal b/sequence-formats.cabal
--- a/sequence-formats.cabal
+++ b/sequence-formats.cabal
@@ -1,6 +1,6 @@
 cabal-version: >=1.10
 name: sequence-formats
-version: 1.3.1
+version: 1.3.2
 license: GPL-3
 license-file: LICENSE
 maintainer: stephan.schiffels@mac.com
@@ -13,6 +13,14 @@
 extra-source-files:
     README.md
     Changelog.md
+    testDat/example.bim
+    testDat/example.eigenstratgeno
+    testDat/example.fasta
+    testDat/example.freqsum
+    testDat/example.histogram.txt
+    testDat/example.ind
+    testDat/example.snp
+    testDat/example.vcf
 
 library
     exposed-modules:
diff --git a/testDat/example.bim b/testDat/example.bim
new file mode 100644
--- /dev/null
+++ b/testDat/example.bim
@@ -0,0 +1,7 @@
+11       rs0000     0.000000            0 A C
+11       rs1111     0.001000       100000 A G
+11       rs2222     0.002000       200000 A T
+11       rs3333     0.003000       300000 C A
+11       rs4444     0.004000       400000 G A
+11       rs5555     0.005000       500000 T A
+11       rs6666     0.006000       600000 G T
diff --git a/testDat/example.eigenstratgeno b/testDat/example.eigenstratgeno
new file mode 100644
--- /dev/null
+++ b/testDat/example.eigenstratgeno
@@ -0,0 +1,7 @@
+11100
+01212
+21101
+09122
+21100
+00191
+22199
diff --git a/testDat/example.fasta b/testDat/example.fasta
new file mode 100644
--- /dev/null
+++ b/testDat/example.fasta
@@ -0,0 +1,10 @@
+>chr1 bla bla bla
+ACCAATTTCCCTTTAATATAAG
+ACCCTTTCGGGGAAA
+>chr2 dsasdfas
+ACTACTACTACTACTACTACTACGGGGG
+AAAAAAAAACCCCCCCCCGGGGGGGG
+>chr3 kflfksja
+ACGACGACGACGGGGTTTAAA
+AAGGGTTTCCTCTCTCTCTGGG
+
diff --git a/testDat/example.freqsum b/testDat/example.freqsum
new file mode 100644
--- /dev/null
+++ b/testDat/example.freqsum
@@ -0,0 +1,8 @@
+#CHROM	POS	REF	ALT	SAMPLE0(2)	SAMPLE1(2)	SAMPLE2(2)	SAMPLE3(1)	SAMPLE4(1)
+11	0	A	C	1	1	1	1	1
+11	100000	A	G	2	1	0	0	0
+11	200000	A	T	0	1	1	1	1
+11	300000	C	A	2	-1	1	0	0
+11	400000	G	A	0	1	1	1	1
+11	500000	T	A	2	2	1	-1	1
+11	600000	G	T	0	0	1	-1	-1
diff --git a/testDat/example.histogram.txt b/testDat/example.histogram.txt
new file mode 100644
--- /dev/null
+++ b/testDat/example.histogram.txt
@@ -0,0 +1,10 @@
+NAMES=EUR,SEA,SIB,CHK,SAM
+N=66,42,44,8,28
+MAX_M=10
+TOTAL_SITES=1146826657
+1,0,0,0,0 773148 6.7e-4 3.6e-6
+0,1,0,0,0 527207 4.5e-4 2.5e-6
+0,0,1,0,0 368640 3.2e-4 2.4e-6
+0,0,0,0,1 213918 1.8e-4 3.6e-6
+2,0,0,0,0 158795 1.3e-4 1.4e-6
+0,2,0,0,0 73241 6.3e-5 7.3e-7
diff --git a/testDat/example.ind b/testDat/example.ind
new file mode 100644
--- /dev/null
+++ b/testDat/example.ind
@@ -0,0 +1,5 @@
+	     SAMPLE0 F       Case
+             SAMPLE1 M       Case
+             SAMPLE2 F    Control
+             SAMPLE3 M    Control
+             SAMPLE4 F    Control
diff --git a/testDat/example.snp b/testDat/example.snp
new file mode 100644
--- /dev/null
+++ b/testDat/example.snp
@@ -0,0 +1,7 @@
+              rs0000  11        0.000000               0 A C
+              rs1111  11        0.001000          100000 A G
+              rs2222  11        0.002000          200000 A T
+              rs3333  11        0.003000          300000 C A
+              rs4444  11        0.004000          400000 G A
+              rs5555  11        0.005000          500000 T A
+              rs6666  11        0.006000          600000 G T
diff --git a/testDat/example.vcf b/testDat/example.vcf
new file mode 100644
--- /dev/null
+++ b/testDat/example.vcf
@@ -0,0 +1,27 @@
+##fileformat=VCFv4.2
+##FILTER=<ID=PASS,Description="All filters passed">
+##samtoolsVersion=1.3+htslib-1.3
+##samtoolsCommand=samtools mpileup -vI -f /projects1/Reference_Genomes/Human/hs37d5/hs37d5.fa -r 1:1-200000 12880A.bam 12881A.bam 12883A.bam 12884A.bam 12885A.bam
+##reference=file:///projects1/Reference_Genomes/Human/hs37d5/hs37d5.fa
+##contig=<ID=1,length=249250621>
+##contig=<ID=2,length=243199373>
+##contig=<ID=3,length=198022430>
+##contig=<ID=4,length=191154276>
+##contig=<ID=5,length=180915260>
+##contig=<ID=hs37d5,length=35477943>
+##ALT=<ID=*,Description="Represents allele(s) other than observed.">
+##INFO=<ID=INDEL,Number=0,Type=Flag,Description="Indicates that the variant is an INDEL.">
+##FORMAT=<ID=PL,Number=G,Type=Integer,Description="List of Phred-scaled genotype likelihoods">
+##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
+##INFO=<ID=AF1,Number=1,Type=Float,Description="Max-likelihood estimate of the first ALT allele frequency (assuming HWE)">
+##INFO=<ID=DP4,Number=4,Type=Integer,Description="Number of high-quality ref-forward , ref-reverse, alt-forward and alt-reverse bases">
+##bcftools_callVersion=1.3+htslib-1.3
+##bcftools_callCommand=call -c -v
+#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	12880A	12881A	12883A	12884A	12885A
+1	10492	.	C	T	15.0302	.	DP=28;PV4=1,1,0.30985,1	GT:PL	0/0:0,3,37	0/0:0,6,67	0/1:51,0,28	0/0:0,54,255	0/0:0,9,83
+1	14907	.	A	G	146.092	.	DP=55.526787;AC1=5;DP4=19,16,8,12;PV4=0.403198,0.000983733,1,0.0348559	GT:PL	0/1:0,0,0	0/0:0,9,42	0/1:51,0,0	0/1:70,0,123	1/1:68,5,0
+1	14930	.	A	G	999	.	DP=61.545999;AC1=6;;FQ=999;PV4=0.602167,0.240103,1,1	GT:PL	0/1:0,3,20	0/1:22,0,47	0/1:70,0,26	0/1:188,0,121	1/1:80,12,0
+2	14933	.	G	A	51.2451	.	DP=60.215796;PV4=0.49427,1,1,1	GT:PL	0/0:0,6,39	0/1:25,0,48	0/0:0,18,118	0/1:69,0,163	0/0:0,12,80
+2	16495	.	G	C	7.29715	.	DP=47.27107;AC1=2;PV4=0.540781,0.244272,1,0.0352549	GT:PL	0/0:0,9,9	0/1:23,3,0	0/0:0,4,9	0/1:27,0,46	0/0:0,9,21
+2	20144	.	G	A	15.7039	.	DP=121;AC1=3;PV4=1,1,1,1	GT:PL	0/0:0,5,81	0/1:33,0,47	0/1:9,0,21	0/0:0,182,122	0/1:18,0,27
+2	30923	rs12345	G	.	110.112	.	DP=5;FQ=-28.9619	GT:PL	1/1:0,0,0	1/1:0,0,0	1/1:40,6,0	1/1:105,9,0	1/1:0,0,0