chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	50966452	50966453	C	CTGAG	19	GENIC	homozygous	59689468
2	50966521	50966522	T	TAC	18	GENIC	heterozygous	59689470
2	50966567	50966568	T	G	39	GENIC	homozygous	58817783
2	50966920	50966921	C	A	48	GENIC	homozygous	59689472
2	50967383	50967384	G	A	55	GENIC	homozygous	58817784
2	50968886	50968887	G	A	67	GENIC	homozygous	59689474
2	50969164	50969165	C	T	45	GENIC	homozygous	59689476
2	50969784	50969785	A	G	40	GENIC	homozygous	58817791
2	50969916	50969917	A	G	40	GENIC	homozygous	58817792
2	50970068	50970069	G	-	40	GENIC	homozygous	58817793
2	50970785	50970787	AT	--	30	GENIC	homozygous	58817795
2	50970786	50970787	T	-	30	GENIC	homozygous	58817796
2	50971018	50971019	G	-	52	GENIC	homozygous	58817797
2	50971594	50971595	G	A	43	GENIC	possibly homozygous	59689478
2	50971642	50971643	T	C	45	GENIC	possibly homozygous	59689480
2	50972059	50972060	C	-	7	GENIC	homozygous	58817799
2	50972356	50972357	G	GT	27	GENIC	possibly homozygous	58817800
2	50973969	50973970	A	AGAGGGAGG	11	GENIC	homozygous	58817806
2	50973990	50973991	G	T	18	GENIC	heterozygous	59689482
2	50973997	50974000	GGA	---	11	GENIC	heterozygous	58817807
2	50973998	50974000	GA	--	10	GENIC	homozygous	58817808
2	50974185	50974186	G	-	60	GENIC	homozygous	59689484
2	50974225	50974226	A	G	64	GENIC	possibly homozygous	58817809
2	50974382	50974383	G	-	49	GENIC	homozygous	59689486