chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	105062766	105062767	T	C	26	GENIC	possibly homozygous	120126067
2	105062987	105062988	G	A	19	GENIC	homozygous	120169517
2	105063022	105063023	A	T	24	GENIC	homozygous	109962102
2	105063440	105063441	T	C	18	GENIC	homozygous	109962104
2	105066770	105066771	T	C	22	GENIC	heterozygous	109962106
2	105068374	105068375	G	A	22	GENIC	homozygous	109962108
2	105071172	105071173	G	T	28	GENIC	homozygous	109962114
2	105071970	105071971	G	A	27	GENIC	homozygous	109962116
2	105072817	105072818	T	A	25	GENIC	homozygous	109962118
2	105073189	105073190	T	G	29	GENIC	homozygous	109962120
2	105074379	105074380	A	T	38	GENIC	homozygous	109962122
2	105075051	105075052	G	A	27	GENIC	homozygous	109962124
2	105075450	105075451	G	A	21	GENIC	homozygous	109962126
2	105076146	105076147	A	T	36	GENIC	homozygous	109962128
2	105076183	105076184	G	A	35	GENIC	homozygous	109962130
2	105076195	105076196	G	C	30	GENIC	homozygous	109962132
2	105076346	105076347	G	C	22	GENIC	homozygous	109962134
2	105076394	105076395	G	A	28	GENIC	homozygous	109962136
2	105076909	105076910	C	A	28	GENIC	homozygous	109962138
2	105077222	105077223	T	A	26	GENIC	homozygous	109962140
2	105077417	105077418	C	T	24	GENIC	homozygous	109962142
2	105078376	105078377	T	C	26	GENIC	homozygous	109962144
2	105080342	105080343	T	G	33	GENIC	homozygous	109962146
2	105080431	105080432	G	C	34	GENIC	homozygous	109962148
2	105081364	105081365	G	A	24	GENIC	homozygous	109962150
2	105081548	105081549	C	T	21	GENIC	homozygous	109962151
2	105081640	105081641	T	C	30	GENIC	homozygous	109962153
2	105082560	105082561	T	G	17	GENIC	homozygous	109962157
2	105084551	105084552	T	A	26	GENIC	homozygous	109962159
2	105084821	105084822	G	T	19	GENIC	heterozygous	120169518
2	105087578	105087579	C	A	22	GENIC	homozygous	109962176
2	105088778	105088779	C	T	34	GENIC	homozygous	109962178
2	105089562	105089563	C	A	29	GENIC	homozygous	109962180