chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	96126771	96126772	C	G	24	GENIC	possibly homozygous	118108490
10	96131999	96132000	A	C	17	GENIC	homozygous	118051571
10	96136559	96136560	A	G	18	GENIC	homozygous	116689367
10	96136661	96136662	A	G	24	GENIC	homozygous	116689375
10	96143050	96143051	A	T	4	GENIC	homozygous	118009790
10	96143056	96143057	G	T	3	GENIC	homozygous	118009791
10	96143110	96143111	C	T	2	GENIC	homozygous	118051575
10	96143116	96143117	A	T	2	GENIC	homozygous	118051577
10	96143122	96143123	C	T	3	GENIC	homozygous	118051579
10	96143134	96143135	C	T	5	GENIC	homozygous	118051580
10	96143138	96143139	C	T	5	GENIC	homozygous	118051582
10	96143142	96143143	G	T	5	GENIC	homozygous	118051584
10	96143146	96143147	G	T	6	GENIC	homozygous	118051586
10	96143150	96143151	C	T	6	GENIC	homozygous	118051587
10	96143154	96143155	G	T	8	GENIC	homozygous	118009793
10	96143166	96143167	C	T	17	GENIC	homozygous	118009794
10	96158657	96158658	A	T	30	GENIC	heterozygous	118009795
10	96159656	96159657	A	T	46	GENIC	heterozygous	118051589
10	96162327	96162328	G	C	26	GENIC	homozygous	118051591
10	96163866	96163867	G	T	8	GENIC	homozygous	118051592
10	96163870	96163871	C	T	8	GENIC	homozygous	118051594
10	96163871	96163872	A	G	8	GENIC	homozygous	118051596