chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	11880218	11880219	G	A	32	GENIC	homozygous	54181699
7	11882108	11882109	C	T	41	GENIC	homozygous	53789579
7	11883569	11883570	C	CCTGT	45	GENIC	homozygous	53789580
7	11884838	11884839	A	G	9	GENIC	homozygous	53789581
7	11885205	11885206	T	C	6	GENIC	homozygous	53789593
7	11885888	11885889	G	A	26	GENIC	homozygous	53789594
7	11885915	11885916	G	C	26	GENIC	homozygous	53789595
7	11885961	11885962	G	C	33	GENIC	possibly homozygous	53789596
7	11885972	11885973	C	T	38	GENIC	possibly homozygous	53789597
7	11887030	11887031	T	C	26	GENIC	homozygous	53789598
7	11887769	11887770	A	T	29	GENIC	homozygous	53789599
7	11887796	11887797	G	T	30	GENIC	homozygous	53789600
7	11888017	11888018	A	ACACAGCCGCGGCCCAG	44	GENIC	homozygous	53789602
7	11888583	11888584	T	TAC	25	GENIC	homozygous	53789603
7	11888654	11888655	C	T	26	GENIC	homozygous	53789604
7	11888824	11888825	G	A	30	GENIC	homozygous	53789605
7	11888900	11888901	A	G	35	GENIC	homozygous	53789606
7	11889125	11889126	G	T	49	GENIC	homozygous	53789607
7	11889691	11889693	CA	--	25	GENIC	homozygous	53789608
7	11890647	11890648	T	G	22	GENIC	homozygous	53789609
7	11891186	11891187	G	GAAAA	6	GENIC	heterozygous	54954614
7	11891186	11891187	G	GAAAAAAA	6	GENIC	heterozygous	54954616
7	11891200	11891201	C	A	17	GENIC	homozygous	53789610
7	11891285	11891286	G	GAA	8	GENIC	heterozygous	53789611
7	11891285	11891286	G	GA	8	GENIC	heterozygous	54954618
7	11891464	11891465	A	G	29	GENIC	homozygous	53789613
7	11891772	11891773	C	T	37	GENIC	homozygous	53789614
7	11891852	11891853	T	C	26	GENIC	homozygous	53789615
7	11891976	11891977	T	C	29	GENIC	homozygous	53789616