chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	140449138	140449139	A	G	51	GENIC	homozygous	115938696
7	140450582	140450583	A	G	49	GENIC	homozygous	115938697
7	140450993	140450994	A	G	47	GENIC	homozygous	115938698
7	140451011	140451012	C	T	47	GENIC	homozygous	115938699
7	140455199	140455200	C	T	35	GENIC	possibly homozygous	115938700
7	140456602	140456603	G	A	40	GENIC	homozygous	115938701
7	140457575	140457576	A	G	59	GENIC	homozygous	115938702
7	140457607	140457608	A	C	53	GENIC	homozygous	115938703
7	140457695	140457696	T	A	42	GENIC	homozygous	115938704
7	140457831	140457832	G	T	36	GENIC	homozygous	115938705
7	140458146	140458147	C	T	56	GENIC	homozygous	115938706
7	140458171	140458172	G	A	51	GENIC	homozygous	115938707
7	140458485	140458486	G	C	58	GENIC	homozygous	115938708
7	140458879	140458880	T	C	62	GENIC	homozygous	115938709
7	140458893	140458894	G	A	56	GENIC	homozygous	115938710
7	140460127	140460128	T	C	37	GENIC	homozygous	115938711
7	140460500	140460501	A	G	34	GENIC	homozygous	115938712
7	140462035	140462036	T	G	23	GENIC	heterozygous	115938713
7	140462086	140462087	T	A	25	GENIC	homozygous	115938714
7	140462441	140462442	C	T	43	GENIC	homozygous	115938715
7	140462922	140462923	G	C	47	GENIC	homozygous	115938716
7	140463441	140463442	T	C	32	GENIC	homozygous	115938717
7	140465355	140465356	C	T	41	GENIC	homozygous	115938718
7	140465548	140465549	G	T	51	GENIC	homozygous	115938719
7	140465585	140465586	C	T	58	GENIC	homozygous	115938720