chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10540177	10540178	G	C	50	GENIC	homozygous	116493210
10	10540598	10540599	T	C	45	GENIC	homozygous	116493212
10	10540670	10540671	T	C	47	GENIC	possibly homozygous	116493214
10	10541932	10541933	C	A	31	GENIC	homozygous	116493216
10	10542363	10542364	C	A	25	GENIC	homozygous	116493218
10	10542442	10542443	A	G	37	GENIC	possibly homozygous	116493220
10	10542707	10542708	T	A	33	GENIC	homozygous	116493222
10	10544228	10544229	C	T	28	GENIC	homozygous	116493224
10	10544548	10544549	C	T	34	GENIC	homozygous	116493226
10	10546323	10546324	A	G	21	GENIC	homozygous	116493228
10	10547653	10547654	C	A	29	GENIC	homozygous	116493230
10	10547779	10547780	T	C	36	GENIC	homozygous	116493232
10	10548073	10548074	A	G	21	GENIC	homozygous	116493234
10	10548355	10548356	A	T	21	GENIC	homozygous	116493236
10	10548867	10548868	A	C	35	GENIC	homozygous	116493238
10	10548953	10548954	A	G	34	GENIC	homozygous	116493240
10	10549344	10549345	T	C	39	GENIC	homozygous	116493242
10	10550034	10550035	T	C	33	GENIC	homozygous	116493244
10	10550075	10550076	C	G	28	GENIC	homozygous	116493246