chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	70396573	70396574	T	C	9	GENIC	homozygous	116799108
10	70396600	70396601	A	T	20	GENIC	homozygous	116799110
10	70396775	70396776	C	T	20	GENIC	homozygous	116799112
10	70396974	70396975	T	C	12	GENIC	homozygous	116799114
10	70397002	70397003	C	T	15	GENIC	homozygous	116799116
10	70397119	70397120	C	T	22	GENIC	homozygous	116799118
10	70397232	70397233	T	C	14	GENIC	homozygous	116799120
10	70397390	70397391	A	C	9	GENIC	homozygous	116799122
10	70397430	70397431	A	G	9	GENIC	homozygous	116799124
10	70397440	70397441	G	A	8	GENIC	homozygous	116799126
10	70397443	70397444	C	T	10	GENIC	homozygous	116799128
10	70397481	70397482	T	C	11	GENIC	homozygous	116799130
10	70397637	70397638	T	C	19	GENIC	homozygous	116627712
10	70397698	70397699	G	A	23	GENIC	homozygous	116799132
10	70397793	70397794	G	C	21	GENIC	homozygous	116799134
10	70397957	70397958	C	T	17	GENIC	homozygous	116799136
10	70398148	70398149	G	T	10	GENIC	homozygous	116799138
10	70398212	70398213	C	T	10	GENIC	homozygous	116799142
10	70398687	70398688	T	G	32	GENIC	homozygous	116799148
10	70398724	70398725	C	T	25	GENIC	homozygous	116799150
10	70398815	70398816	T	G	17	GENIC	homozygous	116627714
10	70399187	70399188	A	G	16	GENIC	homozygous	116627716
10	70399508	70399509	C	G	5	GENIC	homozygous	116799152
10	70399585	70399586	A	T	7	GENIC	homozygous	126489039
10	70399586	70399587	C	T	5	GENIC	homozygous	126489040
10	70399676	70399677	G	A	29	GENIC	heterozygous	116799154