chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	1439974	1439975	A	G	14	GENIC	possibly homozygous	50001069
12	1441386	1441387	C	T	7	GENIC	possibly homozygous	50393748
12	1445150	1445151	A	C	21	GENIC	possibly homozygous	50001074
12	1445270	1445271	A	T	29	GENIC	possibly homozygous	50001075
12	1445622	1445623	A	G	12	GENIC	possibly homozygous	50001076
12	1447097	1447098	C	T	21	GENIC	possibly homozygous	50001077
12	1447418	1447422	GTGT	----	11	GENIC	homozygous	50001082
12	1447923	1447924	C	T	13	GENIC	homozygous	50393750
12	1448765	1448766	C	CGTGTCTGT	2	GENIC	homozygous	50393752
12	1449557	1449558	T	A	20	GENIC	possibly homozygous	50393754
12	1447390	1447392	GT	--	1	GENIC	homozygous	50503138