chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	9694644	9694645	T	C	20	GENIC	homozygous	115251618
12	9699889	9699890	A	G	17	GENIC	homozygous	115251626
12	9705199	9705200	G	A	11	GENIC	homozygous	115444988
12	9705957	9705958	A	C	22	GENIC	homozygous	115251636
12	9708248	9708249	C	G	28	GENIC	homozygous	115251642
12	9708706	9708707	C	T	26	GENIC	homozygous	115482058
12	9709088	9709089	T	C	42	GENIC	homozygous	115482059
12	9710623	9710624	T	G	2	GENIC	homozygous	115251648
12	9710624	9710625	G	T	2	GENIC	homozygous	115251650
12	9713393	9713394	C	T	18	GENIC	homozygous	115482060
12	9714387	9714388	G	A	27	GENIC	homozygous	115482061
12	9715042	9715043	C	T	23	GENIC	homozygous	115251670
12	9716735	9716736	T	C	20	GENIC	homozygous	115482062
12	9716854	9716855	A	C	17	GENIC	homozygous	115251676
12	9717858	9717859	C	T	25	GENIC	homozygous	115482063
12	9717869	9717870	G	A	23	GENIC	homozygous	115251678
12	9718434	9718435	G	A	30	GENIC	homozygous	115482064
12	9719190	9719191	T	C	47	GENIC	homozygous	115251680
12	9722180	9722181	C	T	19	GENIC	homozygous	115482065
12	9725411	9725412	T	C	32	GENIC	homozygous	115251682
12	9725482	9725483	G	C	21	GENIC	homozygous	115251684