chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10540598	10540599	T	C	35	GENIC	homozygous	116493212
10	10540670	10540671	T	C	35	GENIC	homozygous	116493214
10	10541932	10541933	C	A	19	GENIC	homozygous	116493216
10	10542363	10542364	C	A	39	GENIC	homozygous	116493218
10	10542442	10542443	A	G	33	GENIC	homozygous	116493220
10	10542707	10542708	T	A	28	GENIC	homozygous	116493222
10	10544228	10544229	C	T	27	GENIC	homozygous	116493224
10	10544548	10544549	C	T	18	GENIC	homozygous	116493226
10	10546323	10546324	A	G	35	GENIC	homozygous	116493228
10	10547653	10547654	C	A	27	GENIC	homozygous	116493230
10	10547779	10547780	T	C	33	GENIC	homozygous	116493232
10	10548073	10548074	A	G	36	GENIC	possibly homozygous	116493234
10	10548355	10548356	A	T	23	GENIC	homozygous	116493236
10	10548867	10548868	A	C	34	GENIC	homozygous	116493238
10	10548953	10548954	A	G	33	GENIC	homozygous	116493240
10	10549344	10549345	T	C	33	GENIC	homozygous	116493242
10	10550075	10550076	C	G	7	GENIC	homozygous	116493246