chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	250835392	250835393	A	G	34	GENIC	homozygous	110380046
2	250835672	250835673	T	G	74	GENIC	homozygous	110380048
2	250835882	250835883	C	T	60	GENIC	possibly homozygous	110380050
2	250835893	250835894	A	G	56	GENIC	homozygous	110380052
2	250836107	250836108	G	C	22	GENIC	homozygous	110380054
2	250836179	250836180	A	G	31	GENIC	possibly homozygous	110380056
2	250837145	250837146	A	G	37	GENIC	homozygous	110380058
2	250837185	250837186	T	C	32	GENIC	possibly homozygous	110380060
2	250837314	250837315	C	A	47	GENIC	possibly homozygous	110380062
2	250837600	250837601	G	T	38	GENIC	homozygous	110380064
2	250837693	250837694	C	A	47	GENIC	possibly homozygous	110380066
2	250838143	250838144	T	A	27	GENIC	homozygous	110380068
2	250838913	250838914	A	G	29	GENIC	possibly homozygous	110380070
2	250839000	250839001	C	T	25	GENIC	homozygous	110380072
2	250839144	250839145	T	C	36	GENIC	heterozygous	110380074
2	250839154	250839155	G	A	34	GENIC	heterozygous	110380076
2	250839301	250839302	C	A	27	GENIC	possibly homozygous	110380078
2	250839366	250839367	T	C	33	GENIC	homozygous	110380080
2	250839449	250839450	G	C	31	GENIC	homozygous	110380082
2	250841907	250841908	C	A	33	GENIC	homozygous	110380084