chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	115521377	115521378	T	C	38	GENIC	homozygous	136264963
2	115524366	115524369	GGA		29	GENIC	homozygous	135937863
2	115527241	115527242	A	T	39	GENIC	homozygous	136264974
2	115525170	115525171	G	C	41	GENIC	homozygous	144316568
2	115531145	115531146	T		15	GENIC	homozygous	140859372
2	115531177	115531178	A		9	GENIC	heterozygous	403017011
2	115531191	115531192	A	G	9	GENIC	heterozygous	403017016
2	115531174	115531175	A		15	GENIC	heterozygous	403017009
2	115531174	115531175	A	G	15	GENIC	homozygous	403017010
2	115531177	115531178	A	G	9	GENIC	heterozygous	403017012
2	115531185	115531186	A		13	GENIC	heterozygous	403017013
2	115531185	115531186	A	G	13	GENIC	homozygous	403017014
2	115531191	115531192	A		9	GENIC	heterozygous	403017015
2	115531193	115531194	C		9	GENIC	heterozygous	403017017
2	115531193	115531194	C	G	9	GENIC	heterozygous	403017018
2	115531857	115531858	T	C	46	GENIC	homozygous	136264984