chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	15091051	15091052	T	C	29	GENIC	homozygous	116497622
10	15091068	15091069	T	C	26	GENIC	homozygous	116497624
10	15091101	15091102	T	C	27	GENIC	homozygous	116497626
10	15091364	15091365	C	T	38	GENIC	homozygous	116497628
10	15091366	15091367	G	T	37	GENIC	homozygous	116497630
10	15091644	15091645	A	G	36	GENIC	homozygous	116497632
10	15091836	15091837	C	T	41	GENIC	homozygous	116497634
10	15091887	15091888	A	G	43	GENIC	homozygous	116737562
10	15091961	15091962	A	G	42	GENIC	homozygous	116737563
10	15092074	15092075	C	T	27	GENIC	homozygous	116737564
10	15092075	15092076	A	G	27	GENIC	homozygous	116737565
10	15092089	15092090	A	C	28	GENIC	homozygous	116737566
10	15092134	15092135	A	C	35	GENIC	homozygous	116497640
10	15094982	15094983	G	A	38	GENIC	homozygous	116737567
10	15095037	15095038	A	G	38	GENIC	homozygous	116497698
10	15095122	15095123	A	G	32	GENIC	homozygous	116497700
10	15096760	15096761	T	G	47	GENIC	homozygous	116497704