chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	250835015	250835016	T	C	13	GENIC	possibly homozygous	111292809
2	250835392	250835393	A	G	11	GENIC	homozygous	110380046
2	250835882	250835883	C	T	13	GENIC	homozygous	110380050
2	250835893	250835894	A	G	12	GENIC	homozygous	110380052
2	250836107	250836108	G	C	6	GENIC	homozygous	110380054
2	250837185	250837186	T	C	12	GENIC	homozygous	110380060
2	250837600	250837601	G	T	10	GENIC	homozygous	110380064
2	250838913	250838914	A	G	11	GENIC	homozygous	110380070
2	250837693	250837694	C	A	11	GENIC	homozygous	110380066
2	250838143	250838144	T	A	12	GENIC	homozygous	110380068
2	250839366	250839367	T	C	7	GENIC	homozygous	110380080
2	250839449	250839450	G	C	7	GENIC	homozygous	110380082
2	250841907	250841908	C	A	8	GENIC	homozygous	110380084