chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	11828466	11828467	G	A	25	GENIC	homozygous	53789460
7	11829012	11829013	G	T	29	GENIC	homozygous	53789461
7	11829027	11829028	C	CG	24	GENIC	homozygous	53789462
7	11830455	11830456	T	TC	14	GENIC	homozygous	53789463
7	11831494	11831495	C	T	11	GENIC	possibly homozygous	53789464
7	11831498	11831499	C	G	10	GENIC	possibly homozygous	54181683
7	11831514	11831515	C	T	17	GENIC	homozygous	53789466
7	11831526	11831527	C	T	21	GENIC	homozygous	53789467
7	11832722	11832723	A	T	47	GENIC	homozygous	53789468
7	11833215	11833216	A	AGAGGAC	16	GENIC	homozygous	53789469
7	11833916	11833917	C	T	32	GENIC	possibly homozygous	53789470
7	11834565	11834566	T	G	54	GENIC	homozygous	53789471
7	11835051	11835052	T	C	31	GENIC	homozygous	53789472
7	11836669	11836670	G	A	48	GENIC	homozygous	53789473
7	11837735	11837736	C	T	44	GENIC	homozygous	53789474
7	11839496	11839497	A	G	26	GENIC	homozygous	53789475
7	11842474	11842475	C	T	25	GENIC	homozygous	53789476
7	11842950	11842951	A	G	49	GENIC	homozygous	53789477
7	11843043	11843051	TGTCATGC	--------	17	GENIC	heterozygous	53789478
7	11843072	11843073	G	C	25	GENIC	heterozygous	53789479
7	11843072	11843073	G	GATGTC	22	GENIC	possibly homozygous	53789480
7	11843091	11843092	G	A	28	GENIC	possibly homozygous	53789481
7	11843633	11843634	C	A	32	GENIC	homozygous	53789482
7	11843681	11843682	C	T	26	GENIC	homozygous	53789483