chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39688826	39688827	G	A	29	GENIC	homozygous	52963101
8	39690555	39690556	G	A	13	GENIC	homozygous	52591421
8	39690934	39690935	A	G	31	GENIC	homozygous	52591422
8	39691393	39691394	T	-	4	GENIC	heterozygous	52591428
8	39691604	39691605	C	T	14	GENIC	homozygous	52591429
8	39691742	39691743	C	T	8	GENIC	heterozygous	52963106
8	39692640	39692641	A	G	14	GENIC	possibly homozygous	52591430
8	39694312	39694313	A	G	8	GENIC	heterozygous	53268802
8	39695107	39695108	T	C	19	GENIC	homozygous	52591447
8	39695400	39695401	G	A	9	GENIC	homozygous	52963111
8	39695767	39695768	T	C	19	GENIC	possibly homozygous	52591450
8	39696109	39696110	C	T	17	GENIC	homozygous	53268803
8	39696400	39696401	G	GT	1	GENIC	homozygous	52591452
8	39696568	39696569	A	G	12	GENIC	possibly homozygous	52591453
8	39697196	39697215	TCCCTCCCCTCCCCTCCCC	-------------------	2	GENIC	heterozygous	53363211
8	39697481	39697482	A	G	23	GENIC	possibly homozygous	52591455
8	39699967	39699968	C	T	20	GENIC	homozygous	52591460
8	39700512	39700513	C	-	8	GENIC	heterozygous	52591462
8	39702186	39702187	G	A	7	GENIC	possibly homozygous	53268804
8	39702312	39702315	TCC	---	2	GENIC	homozygous	52591465
8	39702415	39702416	G	GAA	8	GENIC	homozygous	52591466
8	39703327	39703328	G	A	27	GENIC	possibly homozygous	53268805
8	39703866	39703869	CCC	---	4	GENIC	homozygous	53268806