chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	70135172	70135173	G	T	17	GENIC	possibly homozygous	116627161
10	70136071	70136072	T	C	68	GENIC	homozygous	116627163
10	70136813	70136817	TGTC		51	GENIC	homozygous	128828819
10	70141862	70141862		A	62	GENIC	homozygous	128828820
10	70144623	70144624	T	G	54	GENIC	homozygous	116627165
10	70147090	70147091	G	A	73	GENIC	homozygous	116627167
10	70151102	70151103	A		46	GENIC	homozygous	128828821
10	70151296	70151297	A	G	60	GENIC	homozygous	116627169
10	70151733	70151734	T	C	69	GENIC	homozygous	116627171
10	70154027	70154028	G	C	71	GENIC	homozygous	116627173
10	70156500	70156501	T	C	57	GENIC	homozygous	116627175
10	70156562	70156564	TC		71	GENIC	homozygous	128828822
10	70156763	70156764	A	G	67	GENIC	homozygous	116627177
10	70157025	70157026	C	T	70	GENIC	homozygous	116627179
10	70157218	70157219	T	C	66	GENIC	homozygous	116627181
10	70143299	70143300	G	A	29	GENIC	homozygous	117368911
10	70157694	70157695	C	A	66	GENIC	homozygous	116627183