chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	74340162	74340162		AATC	39	GENIC	homozygous	137960850
7	74340443	74340444	A	G	49	GENIC	homozygous	138120529
7	74340749	74340750	T	C	59	GENIC	homozygous	138120530
7	74341233	74341234	C	T	43	GENIC	homozygous	138120531
7	74343694	74343695	G	A	44	GENIC	homozygous	138120532
7	74345723	74345724	C	T	40	GENIC	homozygous	138120533
7	74347956	74347956		T	55	GENIC	possibly homozygous	137960851
7	74348126	74348127	C	T	56	GENIC	homozygous	138120534
7	74349188	74349189	A		42	GENIC	homozygous	137960852
7	74349432	74349433	C	T	45	GENIC	homozygous	138120535
7	74349778	74349779	C	T	60	GENIC	homozygous	138120536
7	74350641	74350642	C	A	49	GENIC	homozygous	138120537
7	74351111	74351112	G	A	55	GENIC	homozygous	138120538
7	74344358	74344359	T	C	9	GENIC	homozygous	154464334
7	74344358	74344359	T		9	GENIC	heterozygous	403215054
7	74351143	74351144	C	G	53	GENIC	homozygous	138120539
7	74352247	74352248	C	T	57	GENIC	homozygous	138120540
7	74353700	74353701	T	A	26	GENIC	possibly homozygous	138120541
7	74354642	74354643	T	C	48	GENIC	possibly homozygous	138120542
7	74356791	74356792	T	C	38	GENIC	homozygous	138120543
7	74357796	74357797	G	A	58	GENIC	homozygous	138120544
7	74360117	74360118	G	A	51	GENIC	homozygous	138120545
7	74361172	74361173	C	T	53	GENIC	homozygous	138120546
7	74363122	74363122		A	40	GENIC	possibly homozygous	137960853
7	74364818	74364819	A	G	33	GENIC	homozygous	138120547
7	74366211	74366212	T	C	47	GENIC	homozygous	138120548
7	74366664	74366665	A	G	54	GENIC	homozygous	138120549
7	74369152	74369153	A	T	54	GENIC	homozygous	138120550
7	74370326	74370327	G	A	56	GENIC	homozygous	138120551
7	74370732	74370733	T	C	48	GENIC	homozygous	138120552
7	74371069	74371070	C	A	42	GENIC	homozygous	138120553
7	74372444	74372445	A	G	55	GENIC	homozygous	138120554