chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40538666	40538667	C	T	20	GENIC	homozygous	115328364
12	40539761	40539762	G	A	15	GENIC	homozygous	115328366
12	40540705	40540706	G	C	13	GENIC	homozygous	115441583
12	40541039	40541040	C	T	26	GENIC	homozygous	115441584
12	40541900	40541901	G	T	16	GENIC	homozygous	115328370
12	40543218	40543219	C	T	24	GENIC	homozygous	115441585
12	40543301	40543302	G	A	20	GENIC	homozygous	115441586
12	40544195	40544196	A	T	22	GENIC	homozygous	115383871
12	40548227	40548228	G	T	11	GENIC	homozygous	115328380
12	40548229	40548230	G	A	11	GENIC	homozygous	115328382
12	40548233	40548234	G	A	13	GENIC	homozygous	115328384
12	40559224	40559225	C	T	13	GENIC	homozygous	115441587
12	40561037	40561038	T	C	33	GENIC	homozygous	115328386
12	40561613	40561614	C	T	19	GENIC	homozygous	115441588
12	40561701	40561702	T	G	23	GENIC	homozygous	115441589
12	40562255	40562256	T	C	25	GENIC	homozygous	115328388
12	40562459	40562460	C	G	21	GENIC	homozygous	115441590
12	40564519	40564520	T	C	19	GENIC	homozygous	115328392
12	40571068	40571069	C	A	18	GENIC	homozygous	115441591
12	40578828	40578829	A	G	20	GENIC	homozygous	115328394
12	40578977	40578978	T	C	17	GENIC	homozygous	115383883
12	40580604	40580605	A	G	18	GENIC	homozygous	115328396
12	40582670	40582671	G	A	20	GENIC	homozygous	115328398
12	40582898	40582899	T	C	22	GENIC	homozygous	115328402
12	40583804	40583805	C	T	17	GENIC	homozygous	115441592
12	40585147	40585148	C	T	14	GENIC	homozygous	115383885
12	40585389	40585390	C	T	11	GENIC	homozygous	115328404
12	40586081	40586082	G	A	16	GENIC	homozygous	115441593
12	40586787	40586788	G	A	25	GENIC	homozygous	115328406
12	40589906	40589907	A	C	21	GENIC	homozygous	115441594
12	40606683	40606684	C	A	20	GENIC	homozygous	115441595
12	40608997	40608998	T	C	22	GENIC	homozygous	115328416