chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	246990039	246990040	C	T	10	GENIC	homozygous	108602183
1	246990046	246990046		C	10	GENIC	homozygous	127501282
1	246990066	246990066		A	12	GENIC	homozygous	127501283
1	246990076	246990076		CC	12	GENIC	homozygous	127501284
1	246990079	246990079		C	13	GENIC	homozygous	127501285
1	246990139	246990140	T		12	GENIC	homozygous	127501286
1	246990140	246990141	A	C	12	GENIC	homozygous	120493859
1	246990149	246990150	A		12	GENIC	homozygous	127501287
1	246990187	246990188	T		13	GENIC	homozygous	127501288
1	246990195	246990195		T	13	GENIC	homozygous	127501289
1	246990253	246990254	A		14	GENIC	homozygous	127501290
1	246990311	246990312	A		12	GENIC	homozygous	127501291
1	246990363	246990364	T	A	4	GENIC	homozygous	120512597
1	246990363	246990363		G	5	GENIC	homozygous	127501292
1	247003773	247003774	A	C	6	GENIC	homozygous	108602192
1	247018590	247018591	G	T	18	GENIC	homozygous	120476742
1	247020291	247020292	T	C	25	GENIC	homozygous	108602245
1	247004051	247004053	CA		2	GENIC	homozygous	131583451
1	246990607	246990608	C		12	GENIC	homozygous	127501293
1	246990654	246990655	T		11	GENIC	homozygous	127501294
1	246990692	246990693	T		17	GENIC	homozygous	127501295
1	247018590	247018590		T	18	GENIC	homozygous	127501308