chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	250601319	250601320	T	A	16	GENIC	homozygous	120176941
2	250601516	250601517	T	C	21	GENIC	homozygous	110379087
2	250603098	250603099	T	C	16	GENIC	homozygous	120163466
2	250603218	250603219	T	G	23	GENIC	homozygous	120163467
2	250605718	250605719	A	G	17	GENIC	homozygous	120163468
2	250609320	250609321	A	G	29	GENIC	homozygous	110379141
2	250615330	250615331	T	G	21	GENIC	homozygous	110379169
2	250617383	250617384	A	G	12	GENIC	homozygous	110379187
2	250617453	250617454	T	C	19	GENIC	homozygous	110379189
2	250622204	250622205	A	G	24	GENIC	homozygous	110379211
2	250624510	250624511	C	T	13	GENIC	homozygous	110379237
2	250625984	250625985	T	C	11	GENIC	homozygous	110379260
2	250627501	250627502	G	A	10	GENIC	homozygous	120163469
2	250627888	250627889	G	A	24	GENIC	homozygous	120163470
2	250628245	250628246	A	C	10	GENIC	heterozygous	125631377
2	250631648	250631649	T	G	12	GENIC	heterozygous	125611370
2	250631649	250631650	T	G	15	GENIC	homozygous	125611371
2	250631715	250631716	G	C	9	GENIC	heterozygous	110635614