chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	31745774	31745775	A	G	22	GENIC	homozygous	403379549
15	31745774	31745775	A		22	GENIC	heterozygous	403379550
15	31745784	31745785	A	G	20	GENIC	homozygous	403379551
15	31745784	31745785	A		20	GENIC	heterozygous	403379552
15	31745788	31745789	A		20	GENIC	homozygous	403379553
15	31745788	31745789	A	G	20	GENIC	heterozygous	403379554
15	31745804	31745805	A	G	22	GENIC	homozygous	139709032
15	31745810	31745811	C		22	GENIC	homozygous	403379555
15	31745810	31745811	C	G	22	GENIC	heterozygous	403379556
15	31745849	31745850	G	A	24	GENIC	homozygous	403379557
15	31745849	31745850	G		24	GENIC	heterozygous	403379558
15	31746414	31746415	C	G	11	GENIC	homozygous	139709033
15	31746418	31746419	C	A	11	GENIC	homozygous	139709034
15	31746418	31746419	C		11	GENIC	heterozygous	403379559
15	31746427	31746428	C	G	11	GENIC	homozygous	139709035
15	31779078	31779079	C	T	9	GENIC	heterozygous	404405146
15	31745810	31745813	CAG		22	GENIC	homozygous	139626389
15	31779056	31779070	CGCGCGCGCGCGCG		9	GENIC	heterozygous	148604071
15	31779070	31779071	C		9	GENIC	heterozygous	404405141
15	31779070	31779071	C	T	9	GENIC	heterozygous	404405142
15	31779076	31779077	C		9	GENIC	heterozygous	404405143
15	31779076	31779077	C	T	9	GENIC	heterozygous	404405144
15	31779078	31779079	C		9	GENIC	heterozygous	404405145
15	31786995	31786997	AG		17	GENIC	heterozygous	145219556
15	31790827	31790828	A	T	13	GENIC	homozygous	139709036
15	31792345	31792346	A	G	27	GENIC	heterozygous	403379561
15	31794558	31794562	AAAT		8	GENIC	heterozygous	147833781
15	31798128	31798129	A		18	GENIC	homozygous	139626390
15	31792301	31792302	A	G	20	GENIC	heterozygous	142487718
15	31792248	31792249	C	G	19	GENIC	heterozygous	147070948
15	31792255	31792256	T	C	18	GENIC	heterozygous	142487716
15	31792295	31792296	C	A	21	GENIC	heterozygous	142487717