chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	107695637	107695638	A	G	34	GENIC	homozygous	115807964
7	107697562	107697563	C	T	43	GENIC	homozygous	115807966
7	107698638	107698639	G	T	57	GENIC	homozygous	115807968
7	107698694	107698695	G	A	39	GENIC	homozygous	115807970
7	107699044	107699045	C	A	40	GENIC	homozygous	115807972
7	107699920	107699921	T	C	42	GENIC	homozygous	115807976
7	107700548	107700549	A	G	53	GENIC	homozygous	115807978
7	107703373	107703374	G	T	24	GENIC	homozygous	115807984
7	107703556	107703557	C	T	56	GENIC	homozygous	115807986
7	107703575	107703576	C	T	53	GENIC	homozygous	115807988
7	107703606	107703607	G	A	48	GENIC	homozygous	115807990
7	107703909	107703910	C	T	43	GENIC	homozygous	115807992
7	107705110	107705111	G	A	36	GENIC	homozygous	115807994
7	107707537	107707538	G	A	44	GENIC	homozygous	115807996
7	107709747	107709748	A	G	48	GENIC	homozygous	115808000
7	107711540	107711541	A	G	36	GENIC	homozygous	115808002
7	107712278	107712279	C	T	32	GENIC	homozygous	115808004
7	107714819	107714820	C	T	39	GENIC	homozygous	115808006
7	107714872	107714873	C	T	47	GENIC	homozygous	115808008
7	107714923	107714924	G	A	38	GENIC	homozygous	115808010
7	107717668	107717669	G	T	34	GENIC	homozygous	115808012
7	107719050	107719051	C	T	47	GENIC	homozygous	115808014
7	107720537	107720538	C	G	32	GENIC	homozygous	115808016
7	107721577	107721578	G	A	44	GENIC	homozygous	115808018
7	107721736	107721737	G	A	55	GENIC	homozygous	115808020
7	107722906	107722907	A	G	44	GENIC	homozygous	115808022
7	107722931	107722932	A	G	41	GENIC	homozygous	115808024