chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	10332802	10332803	T	C	32	GENIC	homozygous	114721362
6	10333857	10333858	T	C	34	GENIC	homozygous	114721364
6	10334197	10334198	T	C	40	GENIC	homozygous	118552285
6	10334198	10334199	C	T	42	GENIC	homozygous	118552286
6	10334208	10334209	A	C	42	GENIC	homozygous	114721366
6	10334466	10334467	C	T	39	GENIC	homozygous	115043735
6	10334474	10334475	C	T	38	GENIC	homozygous	115043736
6	10334475	10334476	T	C	37	GENIC	homozygous	114721368
6	10334868	10334869	C	T	25	GENIC	possibly homozygous	114721370
6	10336627	10336628	G	A	27	GENIC	homozygous	114721372
6	10336934	10336935	T	C	27	GENIC	possibly homozygous	114721374
6	10337368	10337369	T	C	20	GENIC	homozygous	114721376
6	10338454	10338455	A	G	50	GENIC	homozygous	114721378
6	10339019	10339020	A	C	36	GENIC	homozygous	114721380
6	10340910	10340911	A	G	31	GENIC	homozygous	114721382
6	10342250	10342251	T	A	34	GENIC	homozygous	114721384
6	10342967	10342968	C	G	40	GENIC	homozygous	114721388
6	10343041	10343042	C	T	36	GENIC	homozygous	114721390
6	10343061	10343062	A	T	30	GENIC	homozygous	114721392
6	10343393	10343394	T	C	35	GENIC	homozygous	114721394
6	10343407	10343408	T	C	38	GENIC	homozygous	114721396
6	10343651	10343652	A	T	51	GENIC	homozygous	114721398
6	10344168	10344169	T	A	36	GENIC	homozygous	114721400
6	10344207	10344208	A	G	30	GENIC	homozygous	114721402
6	10345102	10345103	G	C	25	GENIC	homozygous	114721420
6	10345353	10345354	T	C	26	GENIC	homozygous	114721422
6	10345358	10345359	G	A	25	GENIC	homozygous	114721424
6	10345498	10345499	G	A	16	GENIC	homozygous	114721426
6	10345704	10345705	C	A	16	GENIC	possibly homozygous	114721428
6	10345770	10345771	A	G	27	GENIC	possibly homozygous	114721430
6	10345772	10345773	T	A	27	GENIC	possibly homozygous	114721432
6	10345917	10345918	G	A	27	GENIC	homozygous	114721434
6	10346130	10346131	G	A	22	GENIC	homozygous	114721436
6	10346237	10346238	A	G	15	GENIC	homozygous	114721437