chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	110251386	110251387	C	T	17	GENIC	homozygous	116720132
10	110251614	110251615	G	T	27	GENIC	homozygous	116910058
10	110251753	110251754	T	A	30	GENIC	homozygous	116720140
10	110251780	110251781	T	G	35	GENIC	homozygous	116720144
10	110252523	110252524	C	G	33	GENIC	homozygous	116910059
10	110252682	110252683	T	C	27	GENIC	homozygous	116720160
10	110252728	110252729	A	G	28	GENIC	homozygous	116720162
10	110252743	110252744	A	G	30	GENIC	homozygous	116720164
10	110252814	110252815	C	T	35	GENIC	homozygous	116910060
10	110253225	110253226	T	C	23	GENIC	homozygous	116910061
10	110253787	110253788	G	A	30	GENIC	homozygous	116910062
10	110253793	110253794	C	T	33	GENIC	homozygous	116910063
10	110254929	110254930	C	T	32	GENIC	homozygous	116720180
10	110255119	110255120	G	A	31	GENIC	homozygous	116720182
10	110256752	110256753	G	A	10	GENIC	homozygous	118013290
10	110256768	110256769	A	G	13	GENIC	heterozygous	118076524
10	110258087	110258088	A	G	24	GENIC	homozygous	116720184
10	110256806	110256807	A	G	12	GENIC	possibly homozygous	118071246