chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97649095	97649096	T	C	23	GENIC	homozygous	116694444
10	97650016	97650017	C	T	40	GENIC	homozygous	116694446
10	97651077	97651078	C	T	30	GENIC	homozygous	116694448
10	97654288	97654289	T	A	35	GENIC	homozygous	116694450
10	97657209	97657210	T	C	19	GENIC	possibly homozygous	116694452
10	97657606	97657607	C	T	7	GENIC	homozygous	116694454
10	97657787	97657788	T	C	24	GENIC	homozygous	116694456
10	97658658	97658659	G	A	51	GENIC	homozygous	116694458
10	97659677	97659678	T	C	42	GENIC	homozygous	116694460
10	97661998	97661999	G	A	25	GENIC	homozygous	116694462
10	97664675	97664676	T	A	23	GENIC	homozygous	116694464
10	97665139	97665140	T	G	33	GENIC	homozygous	116694466
10	97665736	97665737	A	G	36	GENIC	homozygous	116694468
10	97666543	97666544	A	G	39	GENIC	homozygous	116694470
10	97668179	97668180	C	T	32	GENIC	homozygous	116694472
10	97669098	97669099	G	A	35	GENIC	homozygous	116694474
10	97669930	97669931	T	C	44	GENIC	homozygous	116694476
10	97671220	97671221	A	G	36	GENIC	homozygous	116694478
10	97672980	97672981	G	A	45	GENIC	homozygous	116694480
10	97673874	97673875	G	A	40	GENIC	homozygous	116694482
10	97674479	97674480	T	A	42	GENIC	homozygous	116694484
10	97674977	97674978	C	T	35	GENIC	homozygous	116694486
10	97675292	97675293	A	G	28	GENIC	homozygous	116694488
10	97676112	97676113	A	G	33	GENIC	homozygous	116694490
10	97677007	97677008	C	A	47	GENIC	homozygous	116694492
10	97677150	97677151	A	G	47	GENIC	possibly homozygous	116694494
10	97677460	97677461	C	T	53	GENIC	homozygous	116694496
10	97677559	97677560	G	A	54	GENIC	homozygous	116694498
10	97678189	97678190	C	T	56	GENIC	homozygous	116694500
10	97678198	97678199	T	G	52	GENIC	homozygous	116694502
10	97678402	97678403	A	C	51	GENIC	homozygous	116694504
10	97678446	97678447	T	A	44	GENIC	homozygous	116694506
10	97678450	97678451	G	A	43	GENIC	homozygous	116694508