chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	235397477	235397478	G	A	49	GENIC	possibly homozygous	110315086
2	235397519	235397520	T	A	34	GENIC	homozygous	110315088
2	235397720	235397721	T	C	53	GENIC	homozygous	110315090
2	235397792	235397793	A	C	31	GENIC	homozygous	110315092
2	235397915	235397916	A	G	28	GENIC	homozygous	110315097
2	235398095	235398096	A	G	46	GENIC	homozygous	110315099
2	235398309	235398310	T	C	32	GENIC	homozygous	110315101
2	235398384	235398385	G	A	27	GENIC	homozygous	110315105
2	235398471	235398472	T	C	49	GENIC	homozygous	110315107
2	235399800	235399801	T	C	16	GENIC	homozygous	110315117
2	235399963	235399964	G	A	44	GENIC	homozygous	110315119
2	235400397	235400398	C	T	49	GENIC	homozygous	110315125
2	235400547	235400548	G	A	44	GENIC	homozygous	110315127
2	235400553	235400554	G	A	45	GENIC	homozygous	110315129
2	235400774	235400775	T	G	34	GENIC	homozygous	110315137
2	235401049	235401050	A	G	31	GENIC	homozygous	110315139
2	235401077	235401078	G	A	47	GENIC	homozygous	110315141
2	235401787	235401788	C	T	25	GENIC	homozygous	110315151
2	235401898	235401899	A	C	42	GENIC	homozygous	110315153