chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	79637806	79637807	C	T	23	GENIC	homozygous	117047473
8	79638503	79638504	T	C	33	GENIC	homozygous	117047474
8	79639863	79639864	G	A	17	GENIC	homozygous	117047475
8	79639893	79639894	T	A	10	GENIC	possibly homozygous	117047476
8	79640123	79640124	A	G	37	GENIC	homozygous	117047477
8	79640473	79640474	A	G	41	GENIC	homozygous	117047478
8	79640558	79640559	G	A	53	GENIC	heterozygous	117047479
8	79640731	79640732	C	T	35	GENIC	homozygous	117047480
8	79640744	79640745	G	A	33	GENIC	homozygous	117047481
8	79640754	79640755	C	G	30	GENIC	homozygous	117047482
8	79641225	79641226	C	A	33	GENIC	homozygous	117047483
8	79641556	79641557	C	T	32	GENIC	homozygous	117047484
8	79641834	79641835	T	C	38	GENIC	homozygous	117047485
8	79642660	79642661	C	T	31	GENIC	homozygous	117047486
8	79642910	79642911	T	C	9	GENIC	homozygous	117047487
8	79643094	79643095	T	C	27	GENIC	homozygous	117047488
8	79643256	79643257	A	T	33	GENIC	possibly homozygous	117047489
8	79643415	79643416	A	G	41	GENIC	possibly homozygous	117047490
8	79643450	79643451	A	G	31	GENIC	homozygous	117047491
8	79643573	79643574	A	G	42	GENIC	possibly homozygous	117047492
8	79644739	79644740	T	C	28	GENIC	homozygous	117047493
8	79645353	79645354	G	C	33	GENIC	homozygous	117047494
8	79645645	79645646	T	C	13	GENIC	homozygous	117047495
8	79645853	79645854	T	C	42	GENIC	homozygous	117047496
8	79645881	79645882	G	A	35	GENIC	homozygous	117047497
8	79646689	79646690	G	A	20	GENIC	possibly homozygous	117047498
8	79646949	79646950	G	T	30	GENIC	homozygous	117047499
8	79647099	79647100	T	G	13	GENIC	possibly homozygous	117047500
8	79648504	79648505	A	C	30	GENIC	homozygous	117047501
8	79648735	79648736	A	G	27	GENIC	homozygous	117047502
8	79648852	79648853	G	A	15	GENIC	homozygous	117047503
8	79649377	79649378	G	A	34	GENIC	homozygous	117047504
8	79650415	79650416	C	T	15	GENIC	homozygous	117047505
8	79651391	79651392	G	A	25	GENIC	homozygous	117047506
8	79651631	79651632	G	T	16	GENIC	homozygous	117047507