chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	62656233	62656234	C	A	32	GENIC	homozygous	116614073
10	62657624	62657625	C	T	34	GENIC	homozygous	116939757
10	62657699	62657700	T	C	33	GENIC	homozygous	116614075
10	62657817	62657818	A	T	35	GENIC	homozygous	116614077
10	62657901	62657902	C	T	38	GENIC	homozygous	116939759
10	62658325	62658326	A	G	41	GENIC	homozygous	116939761
10	62659218	62659219	G	A	38	GENIC	homozygous	116939763
10	62659302	62659303	C	T	40	GENIC	homozygous	116939765
10	62659716	62659717	G	A	21	GENIC	homozygous	116890950
10	62661102	62661103	T	C	27	GENIC	homozygous	116939767
10	62661390	62661391	G	A	40	GENIC	possibly homozygous	116890952
10	62661391	62661392	T	C	40	GENIC	possibly homozygous	116939769
10	62661486	62661487	G	A	35	GENIC	homozygous	116939771
10	62661561	62661562	C	T	28	GENIC	homozygous	116890954
10	62661632	62661633	A	C	26	GENIC	homozygous	116791159
10	62661682	62661683	G	C	31	GENIC	homozygous	116614081
10	62661785	62661786	G	A	38	GENIC	homozygous	116614085
10	62661796	62661797	T	C	35	GENIC	homozygous	116939773
10	62661836	62661837	G	T	30	GENIC	homozygous	116890966
10	62662340	62662341	G	T	29	GENIC	homozygous	116890968
10	62662673	62662674	G	A	37	GENIC	homozygous	116890970
10	62663171	62663172	C	T	41	GENIC	homozygous	116890972