chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40588324	40588325	C	G	71	GENIC	homozygous	147595652
12	40588883	40588884	T	C	69	GENIC	homozygous	147595653
12	40588952	40588953	A	G	59	GENIC	homozygous	147595654
12	40589033	40589034	G	A	49	GENIC	homozygous	147595655
12	40589047	40589049	CT		49	GENIC	homozygous	147590280
12	40590068	40590069	A	G	66	GENIC	homozygous	147595656
12	40590106	40590107	A	T	71	GENIC	homozygous	139143345
12	40590604	40590605	C	T	64	GENIC	homozygous	147595657
12	40590766	40590772	GTGAAC		74	GENIC	homozygous	147590281
12	40591641	40591642	T	C	71	GENIC	homozygous	139143347
12	40592059	40592060	A	G	66	GENIC	homozygous	139143348
12	40592671	40592672	G	A	67	GENIC	homozygous	147595658
12	40592980	40592981	A	G	76	GENIC	homozygous	147595659
12	40593075	40593076	A	G	79	GENIC	possibly homozygous	147595660
12	40593109	40593110	C	T	76	GENIC	possibly homozygous	147595661
12	40593363	40593364	G	A	54	GENIC	homozygous	147595662
12	40593474	40593475	T	C	57	GENIC	homozygous	139143350
12	40593532	40593533	G	A	55	GENIC	homozygous	147595663
12	40595077	40595078	G	C	65	GENIC	possibly homozygous	139143351
12	40595925	40595926	C	T	60	GENIC	possibly homozygous	139143353
12	40596016	40596018	GC		13	GENIC	heterozygous	147590282
12	40597792	40597793	G	A	55	GENIC	homozygous	147595664
12	40598393	40598394	T	C	63	GENIC	homozygous	139143356
12	40596022	40596023	A	G	13	GENIC	heterozygous	403645807
12	40596018	40596019	G	A	13	GENIC	heterozygous	154748902
12	40596020	40596021	A	G	13	GENIC	heterozygous	154748903
12	40596018	40596019	G		13	GENIC	heterozygous	403645804
12	40596020	40596021	A		13	GENIC	heterozygous	403645805
12	40596022	40596023	A		13	GENIC	heterozygous	403645806