chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	79691555	79691556	G	A	40	GENIC	homozygous	117047528
8	79691675	79691676	T	A	50	GENIC	homozygous	116844704
8	79694252	79694253	C	T	52	GENIC	homozygous	117047529
8	79695660	79695670	CCTGTATATT		50	GENIC	homozygous	131050500
8	79696384	79696385	A		72	GENIC	homozygous	131050501
8	79697208	79697208		T	37	GENIC	homozygous	131050502
8	79699704	79699705	G	A	58	GENIC	homozygous	117047530
8	79702434	79702447	CCCAGGCCTCGAT		40	GENIC	homozygous	131050503
8	79703403	79703404	A	C	10	GENIC	heterozygous	134015766
8	79705894	79705895	A	G	18	GENIC	homozygous	116844710
8	79708440	79708441	A	G	23	GENIC	homozygous	116844713
8	79708747	79708748	T	C	38	GENIC	homozygous	117047531
8	79709326	79709327	A	G	47	GENIC	homozygous	116844714
8	79710909	79710910	T	A	44	GENIC	possibly homozygous	117047532
8	79711046	79711062	CAGTAATCCTCCGAGG		58	GENIC	possibly homozygous	131050504
8	79713779	79713779		A	32	GENIC	possibly homozygous	131050505
8	79714424	79714425	T	C	47	GENIC	homozygous	116844715
8	79714502	79714503	G	T	33	GENIC	homozygous	116844716