chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	34993781	34993782	A	C	30	GENIC	homozygous	139135306
12	34995324	34995325	C	T	43	GENIC	homozygous	139135307
12	34998047	34998048	G	A	33	GENIC	homozygous	147004016
12	34996192	34996196	TTTA		32	GENIC	homozygous	139053607
12	35000377	35000378	A	G	36	GENIC	homozygous	139135310
12	35001443	35001444	C	A	46	GENIC	homozygous	147004017
12	35001571	35001572	C	T	35	GENIC	homozygous	147004018
12	35001828	35001829	T	C	46	GENIC	homozygous	147004019
12	35002581	35002582	A	C	54	GENIC	homozygous	139135312
12	35002726	35002727	G	C	44	GENIC	homozygous	147004020
12	35004236	35004236		CAGGTCT	43	GENIC	homozygous	139053611
12	35005433	35005434	G	A	42	GENIC	homozygous	144435640
12	35008029	35008030	T	C	40	GENIC	possibly homozygous	145217360
12	35008098	35008099	C	T	49	GENIC	possibly homozygous	144435645
12	35008424	35008425	T	C	10	GENIC	homozygous	139135316
12	35008570	35008574	TGAA		32	GENIC	possibly homozygous	139053613
12	35009021	35009022	G	A	33	GENIC	homozygous	147004021
12	35009383	35009384	C	T	41	GENIC	homozygous	147004022
12	35010924	35010925	G	A	45	GENIC	homozygous	147004023
12	35011274	35011275	T	G	40	GENIC	homozygous	139135319