chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	113699435	113699436	C	G	20	GENIC	homozygous	117427313
9	113699468	113699469	G	T	20	GENIC	homozygous	117427314
9	113699511	113699512	G	T	21	GENIC	homozygous	117645479
9	113699513	113699514	A	T	21	GENIC	homozygous	117427316
9	113699522	113699523	A	T	23	GENIC	homozygous	117427317
9	113699532	113699533	C	A	20	GENIC	homozygous	117427318
9	113699546	113699547	G	C	11	GENIC	homozygous	117831328
9	113699556	113699557	C	G	10	GENIC	homozygous	117427319
9	113699573	113699574	T	A	8	GENIC	homozygous	117645480
9	113699577	113699578	T	A	8	GENIC	homozygous	117645481
9	113699582	113699583	A	C	8	GENIC	homozygous	117427322
9	113699584	113699585	G	C	8	GENIC	homozygous	117427323
9	113699591	113699592	C	G	8	GENIC	homozygous	117427324
9	113699609	113699610	A	C	3	GENIC	homozygous	117645482
9	113716969	113716970	C	T	17	GENIC	possibly homozygous	117427325
9	113721098	113721099	G	T	17	GENIC	possibly homozygous	117427326
9	113721768	113721769	A	C	42	GENIC	homozygous	117645483
9	113724790	113724791	C	G	28	GENIC	homozygous	117645484
9	113725541	113725542	T	C	27	GENIC	homozygous	117645485
9	113726410	113726411	T	C	29	GENIC	homozygous	117645486
9	113726530	113726531	T	C	46	GENIC	homozygous	117645487
9	113726705	113726706	G	T	38	GENIC	homozygous	117645488
9	113727583	113727584	A	G	33	GENIC	homozygous	117645489
9	113727586	113727587	T	C	37	GENIC	homozygous	117645490
9	113728807	113728808	G	A	34	GENIC	homozygous	117645491
9	113729604	113729605	C	G	37	GENIC	homozygous	117645492
9	113729984	113729985	T	C	30	GENIC	possibly homozygous	117645493
9	113730550	113730551	T	C	30	GENIC	homozygous	117645494
9	113730578	113730579	G	A	38	GENIC	homozygous	117645495
9	113730679	113730680	G	T	55	GENIC	homozygous	117645496
9	113730787	113730788	T	C	71	GENIC	possibly homozygous	117645497
9	113730983	113730984	T	G	51	GENIC	homozygous	117645498
9	113732080	113732081	A	G	41	GENIC	homozygous	117645499