chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	10333857	10333858	T	C	9	GENIC	homozygous	114721364
6	10334868	10334869	C	T	10	GENIC	homozygous	114721370
6	10336627	10336628	G	A	12	GENIC	homozygous	114721372
6	10336934	10336935	T	C	15	GENIC	homozygous	114721374
6	10337368	10337369	T	C	11	GENIC	homozygous	114721376
6	10338454	10338455	A	G	20	GENIC	possibly homozygous	114721378
6	10339019	10339020	A	C	15	GENIC	homozygous	114721380
6	10340910	10340911	A	G	31	GENIC	homozygous	114721382
6	10342250	10342251	T	A	4	GENIC	homozygous	114721384
6	10342846	10342847	G	A	14	GENIC	homozygous	114721386
6	10342967	10342968	A	G	11	GENIC	homozygous	126345905
6	10343041	10343042	C	T	20	GENIC	homozygous	114721390
6	10343393	10343394	T	C	4	GENIC	heterozygous	114721394
6	10343407	10343408	T	C	11	GENIC	homozygous	114721396
6	10344168	10344169	T	A	9	GENIC	homozygous	114721400
6	10344207	10344208	A	G	12	GENIC	homozygous	114721402
6	10344754	10344755	C	T	8	GENIC	homozygous	114721416
6	10345022	10345023	A	G	5	GENIC	homozygous	114721418
6	10345102	10345103	G	C	26	GENIC	homozygous	114721420
6	10345353	10345354	T	C	6	GENIC	homozygous	114721422
6	10345358	10345359	G	A	7	GENIC	homozygous	114721424
6	10345498	10345499	G	A	20	GENIC	homozygous	114721426
6	10345704	10345705	C	A	28	GENIC	homozygous	114721428
6	10345770	10345771	A	G	10	GENIC	homozygous	114721430
6	10345772	10345773	T	A	17	GENIC	homozygous	114721432
6	10345917	10345918	G	A	15	GENIC	homozygous	114721434
6	10346130	10346131	G	A	21	GENIC	homozygous	114721436
6	10346237	10346238	A	G	17	GENIC	homozygous	114721437