chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	113699435	113699436	C	G	26	GENIC	homozygous	117427313
9	113721768	113721769	A	C	23	GENIC	homozygous	117645483
9	113724790	113724791	C	G	26	GENIC	homozygous	117645484
9	113725541	113725542	T	C	24	GENIC	homozygous	117645485
9	113726410	113726411	T	C	36	GENIC	homozygous	117645486
9	113726530	113726531	T	C	26	GENIC	homozygous	117645487
9	113726705	113726706	G	T	35	GENIC	homozygous	117645488
9	113727583	113727584	A	G	40	GENIC	homozygous	117645489
9	113727586	113727587	T	C	40	GENIC	homozygous	117645490
9	113728807	113728808	G	A	34	GENIC	homozygous	117645491
9	113729604	113729605	C	G	31	GENIC	homozygous	117645492
9	113729984	113729985	T	C	25	GENIC	homozygous	117645493
9	113730550	113730551	T	C	22	GENIC	homozygous	117645494
9	113730578	113730579	G	A	23	GENIC	homozygous	117645495
9	113730679	113730680	G	T	13	GENIC	homozygous	117645496
9	113730787	113730788	T	C	11	GENIC	homozygous	117645497
9	113730983	113730984	T	G	17	GENIC	homozygous	117645498
9	113732080	113732081	A	G	16	GENIC	homozygous	117645499