chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	84645492	84645493	T	G	20	GENIC	homozygous	110946172
2	84645917	84645918	T	C	33	GENIC	homozygous	110946174
2	84646435	84646436	C	T	21	GENIC	homozygous	110946176
2	84649276	84649277	A	G	20	GENIC	homozygous	110946178
2	84651162	84651163	T	C	24	GENIC	homozygous	110946180
2	84657187	84657188	A	G	10	GENIC	homozygous	110946184
2	84658694	84658695	C	A	17	GENIC	possibly homozygous	110946185
2	84659436	84659437	T	A	25	GENIC	homozygous	109886929
2	84659501	84659502	A	G	21	GENIC	homozygous	110946189
2	84659780	84659781	C	T	39	GENIC	homozygous	110946191
2	84660407	84660408	T	C	39	GENIC	homozygous	109886931
2	84661376	84661377	T	C	25	GENIC	homozygous	109886933
2	84662333	84662334	T	C	30	GENIC	homozygous	110946193
2	84665905	84665906	C	T	35	GENIC	homozygous	110946195
2	84665932	84665933	G	A	39	GENIC	homozygous	110946197
2	84665955	84665956	A	G	38	GENIC	homozygous	110946199