chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	81949673	81949674	A	G	31	GENIC	homozygous	116530155
8	81950218	81950219	A	G	38	GENIC	homozygous	116530157
8	81950488	81950489	A	T	30	GENIC	possibly homozygous	117048449
8	81950617	81950618	T	C	29	GENIC	homozygous	116530159
8	81950929	81950930	C	T	57	GENIC	possibly homozygous	116530161
8	81951146	81951147	A	C	2	GENIC	homozygous	117048450
8	81952423	81952424	G	T	38	GENIC	homozygous	117048451
8	81953247	81953248	T	C	24	GENIC	homozygous	117048452
8	81953725	81953726	T	A	30	GENIC	homozygous	116530163
8	81954230	81954231	G	T	33	GENIC	homozygous	117048453
8	81955319	81955320	A	T	46	GENIC	homozygous	116530165
8	81956588	81956589	A	G	25	GENIC	heterozygous	117048454
8	81956544	81956545	C	G	29	GENIC	possibly homozygous	116845004
8	81956677	81956678	A	C	33	GENIC	homozygous	116845005
8	81956826	81956827	A	G	11	GENIC	homozygous	116845006
8	81958068	81958069	A	G	49	GENIC	homozygous	116530167
8	81959222	81959223	A	T	48	GENIC	homozygous	117048455
8	81960168	81960169	C	T	41	GENIC	possibly homozygous	117048456
8	81960478	81960479	T	C	39	GENIC	homozygous	116530171
8	81960578	81960579	C	T	57	GENIC	possibly homozygous	116530173
8	81962546	81962547	A	G	55	GENIC	possibly homozygous	116530177
8	81962838	81962839	C	T	44	GENIC	homozygous	117048457
8	81963186	81963187	G	A	49	GENIC	possibly homozygous	117048458
8	81969365	81969366	G	A	53	GENIC	possibly homozygous	117048459
8	81970259	81970260	G	A	30	GENIC	homozygous	117048460
8	81971268	81971269	G	A	60	GENIC	homozygous	117048461