chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46220058	46220059	T	C	20	GENIC	homozygous	116585259
10	46220105	46220106	T	C	25	GENIC	homozygous	116585261
10	46220218	46220219	C	G	27	GENIC	homozygous	116877618
10	46221166	46221167	C	G	28	GENIC	homozygous	116877620
10	46222002	46222003	T	C	28	GENIC	homozygous	116585263
10	46222506	46222507	T	C	22	GENIC	homozygous	116877622
10	46222546	46222547	G	A	29	GENIC	homozygous	116877624
10	46222825	46222826	G	A	17	GENIC	homozygous	116877626
10	46224635	46224636	A	G	22	GENIC	homozygous	116877628
10	46224772	46224773	A	G	21	GENIC	homozygous	116877630
10	46224788	46224789	A	C	22	GENIC	homozygous	116585267
10	46225025	46225026	A	G	12	GENIC	homozygous	116877632
10	46226107	46226108	G	A	26	GENIC	possibly homozygous	116877634
10	46226185	46226186	C	G	25	GENIC	homozygous	116877636
10	46226393	46226394	C	T	41	GENIC	homozygous	116877638
10	46226899	46226900	A	G	29	GENIC	homozygous	116585271
10	46227030	46227031	A	T	23	GENIC	homozygous	116877640
10	46228027	46228028	A	G	33	GENIC	homozygous	116585273
10	46228030	46228031	G	C	34	GENIC	homozygous	116877642
10	46228503	46228504	T	C	23	GENIC	homozygous	116877644
10	46230219	46230220	G	A	34	GENIC	homozygous	116877646
10	46232175	46232176	T	C	24	GENIC	homozygous	116877651
10	46232593	46232594	T	A	14	GENIC	homozygous	116585283
10	46233564	46233565	T	C	22	GENIC	homozygous	116877653
10	46240528	46240529	A	T	46	GENIC	homozygous	116585291
10	46241858	46241859	T	C	22	GENIC	homozygous	116585293