chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	255120316	255120317	T	-	8	GENIC	homozygous	61325942
1	255121315	255121316	C	A	44	GENIC	possibly homozygous	61325943
1	255121318	255121319	C	A	40	GENIC	possibly homozygous	61325944
1	255121339	255121340	C	CA	45	GENIC	heterozygous	61166058
1	255121344	255121345	G	-	54	GENIC	possibly homozygous	61166059
1	255121378	255121379	A	-	38	GENIC	possibly homozygous	61166060
1	255122021	255122022	A	G	38	GENIC	homozygous	61166062
1	255122822	255122823	G	A	57	GENIC	possibly homozygous	61166064
1	255123782	255123783	T	C	52	GENIC	homozygous	61166065
1	255124206	255124207	C	T	70	GENIC	homozygous	61325945
1	255124429	255124430	A	AACAC	2	GENIC	heterozygous	61166066
1	255124429	255124430	A	AAC	2	GENIC	heterozygous	61325946
1	255124477	255124478	C	CT	13	GENIC	heterozygous	61166067
1	255124478	255124480	CG	--	13	GENIC	heterozygous	61166068
1	255124486	255124487	A	AC	15	GENIC	homozygous	61166069
1	255125188	255125189	G	A	34	GENIC	possibly homozygous	61325947
1	255125300	255125301	C	G	25	GENIC	homozygous	61166070
1	255125338	255125339	C	CGTGT	4	GENIC	homozygous	61325948
1	255126727	255126728	G	T	45	GENIC	homozygous	61166072
1	255128042	255128043	A	G	72	GENIC	homozygous	61166073
1	255128077	255128078	A	-	40	GENIC	possibly homozygous	61166075
1	255128214	255128215	T	C	34	GENIC	homozygous	61166076
1	255128233	255128234	C	-	28	GENIC	homozygous	61325949
1	255129164	255129169	CTCTC	-----	10	GENIC	possibly homozygous	61325950
1	255129196	255129200	CTCC	----	9	GENIC	homozygous	61166077
1	255129607	255129608	A	G	46	GENIC	possibly homozygous	61325951