chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	31745774	31745775	A	G	39	GENIC	homozygous	403379549
15	31745774	31745775	A		39	GENIC	heterozygous	403379550
15	31745784	31745785	A	G	34	GENIC	homozygous	403379551
15	31745784	31745785	A		34	GENIC	heterozygous	403379552
15	31745788	31745789	A		34	GENIC	homozygous	403379553
15	31745788	31745789	A	G	34	GENIC	heterozygous	403379554
15	31745804	31745805	A	G	29	GENIC	homozygous	139709032
15	31745810	31745813	CAG		20	GENIC	possibly homozygous	139626389
15	31745810	31745811	C		20	GENIC	possibly homozygous	403379555
15	31745810	31745811	C	G	20	GENIC	heterozygous	403379556
15	31745849	31745850	G	A	27	GENIC	homozygous	403379557
15	31745849	31745850	G		27	GENIC	heterozygous	403379558
15	31746414	31746415	C	G	14	GENIC	possibly homozygous	139709033
15	31746418	31746419	C	A	13	GENIC	homozygous	139709034
15	31746418	31746419	C		13	GENIC	heterozygous	403379559
15	31746427	31746428	C	G	18	GENIC	homozygous	139709035
15	31790827	31790828	A	T	36	GENIC	homozygous	139709036
15	31798128	31798129	A		26	GENIC	heterozygous	139626390
15	31798137	31798137		AC	27	GENIC	heterozygous	149096267