chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	111673706	111673707	G	A	22	GENIC	homozygous	117919503
8	111675753	111675754	T	A	19	GENIC	homozygous	117919504
8	111677257	111677258	C	T	23	GENIC	homozygous	117919505
8	111677357	111677358	C	T	29	GENIC	homozygous	117919506
8	111677395	111677396	C	T	38	GENIC	homozygous	117919507
8	111677564	111677565	T	C	30	GENIC	homozygous	116648550
8	111676152	111676153	T	C	19	GENIC	homozygous	116648544
8	111676535	111676536	T	C	29	GENIC	homozygous	116648546
8	111676727	111676728	A	C	31	GENIC	homozygous	116648548
8	111677792	111677793	A	G	20	GENIC	homozygous	116648552
8	111678149	111678150	A	G	26	GENIC	homozygous	116648556
8	111678156	111678157	G	C	25	GENIC	homozygous	116648558
8	111678607	111678608	T	C	25	GENIC	homozygous	117919508
8	111679901	111679902	A	C	28	GENIC	possibly homozygous	117919509
8	111680058	111680059	T	C	27	GENIC	homozygous	116648564
8	111681061	111681062	C	T	25	GENIC	homozygous	117919510
8	111681424	111681425	C	T	36	GENIC	homozygous	117919511
8	111682438	111682439	A	G	15	GENIC	homozygous	116648570
8	111682564	111682565	C	G	20	GENIC	homozygous	117919512
8	111683450	111683451	T	C	33	GENIC	homozygous	116648572
8	111684348	111684349	T	G	38	GENIC	homozygous	117919513
8	111685182	111685183	G	A	20	GENIC	homozygous	117919514
8	111685759	111685760	G	A	26	GENIC	homozygous	117919515
8	111687071	111687072	C	G	10	GENIC	homozygous	117919516
8	111684688	111684689	A	G	17	GENIC	homozygous	116648574
8	111684944	111684945	G	A	14	GENIC	homozygous	116648576
8	111685985	111685986	A	G	14	GENIC	homozygous	116648580