chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	91311307	91311308	A	G	17	GENIC	homozygous	116568552
8	91311734	91311735	A	G	19	GENIC	homozygous	117117064
8	91312595	91312596	A	C	27	GENIC	homozygous	116568556
8	91313017	91313018	T	C	20	GENIC	homozygous	117117065
8	91314114	91314115	T	C	20	GENIC	homozygous	116568562
8	91314706	91314707	A	G	28	GENIC	homozygous	117117066
8	91314931	91314932	C	G	36	GENIC	homozygous	116568566
8	91315134	91315135	G	A	24	GENIC	homozygous	116568568
8	91315249	91315250	G	T	21	GENIC	homozygous	116568570
8	91315575	91315576	T	C	30	GENIC	homozygous	116568572
8	91317877	91317878	C	T	31	GENIC	homozygous	116568576
8	91319478	91319479	C	T	22	GENIC	homozygous	116568578
8	91320931	91320932	A	G	28	GENIC	homozygous	116568584
8	91321001	91321002	T	C	27	GENIC	homozygous	116568586
8	91321347	91321348	T	C	32	GENIC	homozygous	116568588
8	91322933	91322934	G	A	18	GENIC	homozygous	116568592
8	91323980	91323981	T	C	27	GENIC	homozygous	116568596
8	91324603	91324604	A	C	20	GENIC	homozygous	116568598
8	91325293	91325294	G	A	36	GENIC	homozygous	116568602
8	91326871	91326872	G	A	27	GENIC	homozygous	117185879
8	91327685	91327686	G	A	23	GENIC	homozygous	116568614
8	91328865	91328866	T	A	29	GENIC	homozygous	116568616
8	91329377	91329378	A	T	40	GENIC	homozygous	116568618
8	91329509	91329510	A	G	25	GENIC	possibly homozygous	116568620
8	91330622	91330623	A	G	32	GENIC	homozygous	116568624
8	91330948	91330949	C	T	27	GENIC	homozygous	117185880
8	91331272	91331273	T	C	27	GENIC	homozygous	117185881
8	91331318	91331319	T	C	18	GENIC	homozygous	116568626
8	91332384	91332385	T	C	29	GENIC	homozygous	117185882
8	91333757	91333758	C	T	26	GENIC	homozygous	117117082
8	91335282	91335283	T	A	30	GENIC	homozygous	117117085
8	91336497	91336498	C	G	35	GENIC	homozygous	117117087
8	91338296	91338297	G	C	24	GENIC	homozygous	117117088
8	91338519	91338520	A	C	13	GENIC	homozygous	117117089