chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	112788636	112788637	C	T	14	GENIC	homozygous	54645845
6	112789009	112789010	A	G	18	GENIC	possibly homozygous	54645847
6	112789265	112789266	C	G	20	GENIC	possibly homozygous	54645849
6	112789972	112789973	A	G	8	GENIC	heterozygous	54645851
6	112791033	112791034	A	T	4	GENIC	homozygous	54645853
6	112791051	112791052	G	GAA	2	GENIC	homozygous	54645855
6	112791297	112791298	G	A	23	GENIC	homozygous	54645857
6	112791600	112791601	C	A	23	GENIC	possibly homozygous	54645859
6	112791833	112791834	C	T	19	GENIC	homozygous	54645861
6	112792357	112792358	G	T	24	GENIC	homozygous	54645867
6	112792385	112792386	T	G	22	GENIC	homozygous	54645869
6	112792611	112792612	A	AT	9	GENIC	homozygous	54645871
6	112792708	112792709	G	A	10	GENIC	homozygous	54645873
6	112792718	112792719	G	C	9	GENIC	homozygous	54645875
6	112792723	112792724	A	G	9	GENIC	homozygous	54645877
6	112792762	112792763	C	T	18	GENIC	homozygous	54645879
6	112792842	112792843	C	T	22	GENIC	possibly homozygous	54645881
6	112793486	112793487	G	A	20	GENIC	homozygous	54645883
6	112794227	112794228	G	C	20	GENIC	possibly homozygous	54645885
6	112794406	112794407	T	TAA	4	GENIC	homozygous	54645887
6	112794526	112794527	T	C	2	GENIC	homozygous	54645895
6	112794735	112794736	C	G	28	GENIC	possibly homozygous	54645897