chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	71176177	71176178	C	T	8	GENIC	homozygous	54446485
7	71176191	71176192	T	C	11	GENIC	possibly homozygous	54446487
7	71176615	71176616	C	T	16	GENIC	possibly homozygous	54446489
7	71177862	71177863	T	-	12	GENIC	possibly homozygous	54446491
7	71178087	71178088	A	G	14	GENIC	homozygous	54446493
7	71179150	71179151	T	TCCTC	5	GENIC	homozygous	53958378
7	71179198	71179199	A	G	15	GENIC	possibly homozygous	53958380
7	71179386	71179387	A	G	10	GENIC	homozygous	53958382
7	71180246	71180247	A	C	6	GENIC	homozygous	53958386
7	71181169	71181170	G	A	12	GENIC	possibly homozygous	54446495
7	71184788	71184789	C	T	9	GENIC	homozygous	53958394
7	71187560	71187561	G	GAAAAAAA	1	GENIC	homozygous	54981888
7	71188556	71188557	G	A	7	GENIC	homozygous	53958402