chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94570834	94570835	T	C	20	GENIC	homozygous	116685570
10	94571660	94571661	T	C	35	GENIC	homozygous	116826687
10	94571733	94571734	G	A	28	GENIC	homozygous	116955121
10	94572512	94572513	A	T	23	GENIC	homozygous	116955123
10	94572671	94572672	G	A	14	GENIC	homozygous	116955125
10	94572731	94572732	T	C	17	GENIC	homozygous	116685592
10	94573032	94573033	G	A	32	GENIC	homozygous	116685594
10	94573527	94573528	G	A	26	GENIC	homozygous	116955127
10	94573906	94573907	C	T	24	GENIC	homozygous	116955129
10	94573917	94573918	T	C	26	GENIC	homozygous	116685604
10	94574481	94574482	A	G	25	GENIC	homozygous	116955131
10	94574590	94574591	G	A	16	GENIC	homozygous	116955133
10	94574624	94574625	G	A	24	GENIC	possibly homozygous	116982990
10	94574984	94574985	T	A	20	GENIC	homozygous	116685606
10	94575251	94575252	T	C	20	GENIC	homozygous	116685610
10	94575673	94575674	A	G	26	GENIC	homozygous	116955135
10	94575699	94575700	A	G	30	GENIC	possibly homozygous	116685616
10	94576051	94576052	G	A	25	GENIC	homozygous	116955137
10	94576491	94576492	C	T	22	GENIC	homozygous	116826691
10	94576521	94576522	T	C	23	GENIC	homozygous	116955139
10	94576736	94576737	C	T	22	GENIC	homozygous	116826693
10	94576874	94576875	C	T	25	GENIC	homozygous	116685624
10	94577587	94577588	C	T	18	GENIC	homozygous	116955141
10	94578890	94578891	C	T	9	GENIC	possibly homozygous	118009305
10	94579572	94579573	T	C	31	GENIC	homozygous	116685632
10	94579770	94579771	T	C	27	GENIC	homozygous	116685634
10	94579938	94579939	A	G	30	GENIC	homozygous	116685636
10	94581010	94581011	C	T	22	GENIC	homozygous	116685642