chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	56068856	56068857	A	G	29	GENIC	homozygous	114807649
6	56068919	56068920	A	G	31	GENIC	homozygous	114807650
6	56068941	56068942	C	G	41	GENIC	possibly homozygous	114807651
6	56068955	56068956	G	C	37	GENIC	homozygous	114807652
6	56069374	56069375	C	T	36	GENIC	homozygous	114807653
6	56069380	56069381	C	T	37	GENIC	homozygous	114807654
6	56069396	56069397	A	T	44	GENIC	homozygous	114807655
6	56069414	56069415	G	T	47	GENIC	possibly homozygous	114807656
6	56069436	56069437	G	C	53	GENIC	homozygous	114807657
6	56069515	56069516	A	G	53	GENIC	homozygous	114807658
6	56070050	56070051	C	T	20	GENIC	homozygous	114807659
6	56070136	56070137	C	T	18	GENIC	homozygous	114807660
6	56070394	56070395	G	T	30	GENIC	homozygous	114807661
6	56070497	56070498	A	C	51	GENIC	possibly homozygous	114807662
6	56070874	56070875	T	C	58	GENIC	homozygous	114807663
6	56070910	56070911	A	T	62	GENIC	homozygous	114807664
6	56070960	56070961	C	T	52	GENIC	homozygous	114807665
6	56071057	56071058	T	G	53	GENIC	homozygous	114807666
6	56071117	56071118	G	A	45	GENIC	homozygous	114807667
6	56071146	56071147	G	T	43	GENIC	homozygous	114807668
6	56071246	56071247	T	C	46	GENIC	homozygous	114807669
6	56071279	56071280	G	A	44	GENIC	possibly homozygous	114807670
6	56071383	56071384	A	G	42	GENIC	homozygous	114807671
6	56071490	56071491	T	G	38	GENIC	homozygous	114807672