chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	44327028	44327029	G	GT	12	GENIC	homozygous	50212547
12	44327036	44327037	T	TTTG	11	GENIC	heterozygous	50334358
12	44327049	44327052	TTA	---	11	GENIC	homozygous	50212548
12	44327074	44327075	T	-	13	GENIC	homozygous	50212549
12	44327145	44327146	C	CAAAA	1	GENIC	homozygous	50212550
12	44327375	44327376	A	-	11	GENIC	homozygous	50212553
12	44327869	44327870	G	GA	12	GENIC	homozygous	50334362
12	44328856	44328857	T	G	42	GENIC	homozygous	50334366
12	44329400	44329401	G	GA	15	GENIC	heterozygous	50385122
12	44327252	44327255	CCC	---	13	GENIC	homozygous	50385120
12	44327420	44327421	A	C	26	GENIC	possibly homozygous	50385121
12	44329595	44329596	C	A	12	GENIC	homozygous	50212559
12	44329835	44329836	T	TGG	18	GENIC	homozygous	50212561
12	44329836	44329837	G	GGGA	22	GENIC	homozygous	50385123
12	44329918	44329919	A	AAC	12	GENIC	heterozygous	50212562
12	44330005	44330006	G	T	22	GENIC	homozygous	50385124
12	44331880	44331893	TCGCCAGGAGCCT	-------------	10	GENIC	homozygous	50385125
12	44333461	44333464	GGG	---	16	GENIC	homozygous	50334380
12	44333579	44333580	A	T	19	GENIC	homozygous	50385126
12	44334173	44334174	T	C	19	GENIC	homozygous	50385127
12	44334421	44334422	T	TACACACAC	10	GENIC	homozygous	50212568
12	44334700	44334701	T	-	14	GENIC	possibly homozygous	50212569
12	44335138	44335139	T	C	28	GENIC	homozygous	50212570
12	44335631	44335632	T	C	22	GENIC	homozygous	50212571
12	44336019	44336020	G	A	14	GENIC	homozygous	50385128
12	44336966	44336967	C	T	25	GENIC	homozygous	50212578
12	44337826	44337827	A	G	28	GENIC	homozygous	50212579
12	44337951	44337952	A	-	12	GENIC	possibly homozygous	50212580
12	44338029	44338032	GTT	---	9	GENIC	homozygous	50212581
12	44339652	44339653	G	A	23	GENIC	homozygous	50385129
12	44340583	44340585	AA	--	18	GENIC	homozygous	50212583
12	44341808	44341809	C	T	22	GENIC	homozygous	50212586
12	44341876	44341877	A	G	26	GENIC	homozygous	50212587