chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	44327074	44327075	T	-	1	GENIC	homozygous	50212549
12	44327252	44327255	CCC	---	2	GENIC	homozygous	50385120
12	44327420	44327421	A	C	13	GENIC	homozygous	50385121
12	44328856	44328857	T	G	6	GENIC	homozygous	50334366
12	44329400	44329401	G	GA	1	GENIC	homozygous	50385122
12	44329595	44329596	C	A	9	GENIC	heterozygous	50212559
12	44329836	44329837	G	GGGA	2	GENIC	homozygous	50385123
12	44330005	44330006	G	T	20	GENIC	possibly homozygous	50385124
12	44333461	44333464	GGG	---	1	GENIC	homozygous	50334380
12	44333579	44333580	A	T	12	GENIC	homozygous	50385126
12	44334173	44334174	T	C	21	GENIC	homozygous	50385127
12	44335138	44335139	T	C	19	GENIC	heterozygous	50212570
12	44335631	44335632	T	C	4	GENIC	homozygous	50212571
12	44336966	44336967	C	T	9	GENIC	homozygous	50212578
12	44337826	44337827	A	G	19	GENIC	possibly homozygous	50212579
12	44337950	44337953	AAA	---	1	GENIC	homozygous	50544995
12	44338029	44338032	GTT	---	1	GENIC	homozygous	50212581
12	44339652	44339653	G	A	10	GENIC	homozygous	50385129
12	44340582	44340585	AAA	---	1	GENIC	homozygous	50470077
12	44341808	44341809	C	T	13	GENIC	homozygous	50212586
12	44341876	44341877	A	G	8	GENIC	homozygous	50212587