chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	126424156	126424157	C	T	24	GENIC	homozygous	116304086
7	126424428	126424429	G	T	20	GENIC	homozygous	115873477
7	126426413	126426414	C	T	28	GENIC	homozygous	115873481
7	126426495	126426496	C	T	26	GENIC	homozygous	115873483
7	126426666	126426667	C	T	26	GENIC	homozygous	115873485
7	126426670	126426671	T	C	25	GENIC	homozygous	115873487
7	126426905	126426906	G	A	17	GENIC	homozygous	115873491
7	126427075	126427076	T	C	20	GENIC	homozygous	115873493
7	126427494	126427495	A	G	25	GENIC	homozygous	115873495
7	126427700	126427701	G	A	23	GENIC	homozygous	115873497
7	126430070	126430071	C	A	29	GENIC	homozygous	116304087
7	126430491	126430492	T	C	25	GENIC	homozygous	115873501
7	126432062	126432063	G	A	20	GENIC	homozygous	115873503
7	126432160	126432161	G	A	25	GENIC	homozygous	115873505
7	126433596	126433597	A	G	24	GENIC	homozygous	115873509
7	126435437	126435438	A	G	28	GENIC	homozygous	116304088
7	126436302	126436303	A	G	19	GENIC	homozygous	115873513
7	126438379	126438380	G	A	37	GENIC	homozygous	116304090
7	126444415	126444416	T	C	19	GENIC	homozygous	116304091
7	126448671	126448672	C	T	42	GENIC	homozygous	115873539
7	126449446	126449447	A	G	21	GENIC	homozygous	115873543
7	126451101	126451102	C	T	24	GENIC	homozygous	115873547
7	126451316	126451317	G	A	23	GENIC	homozygous	116304094
7	126453095	126453096	A	T	21	GENIC	homozygous	115873549
7	126453224	126453225	G	A	29	GENIC	homozygous	115873551
7	126454193	126454194	T	C	20	GENIC	homozygous	115873553
7	126454476	126454477	G	T	23	GENIC	homozygous	115873555
7	126455421	126455422	A	G	39	GENIC	homozygous	115873557
7	126455499	126455500	G	A	37	GENIC	homozygous	116304095
7	126456060	126456061	A	G	26	GENIC	homozygous	115873559
7	126456806	126456807	A	G	38	GENIC	homozygous	115873561
7	126458300	126458301	G	A	36	GENIC	homozygous	116304096
7	126458598	126458599	G	A	31	GENIC	homozygous	115873563
7	126459208	126459209	C	T	19	GENIC	homozygous	118286580
7	126463613	126463614	A	G	21	GENIC	homozygous	115873567