chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	105061277	105061278	T	C	18	GENIC	homozygous	110580358
2	105061315	105061316	C	T	25	GENIC	homozygous	110580360
2	105062485	105062486	A	G	22	GENIC	homozygous	110580362
2	105063022	105063023	A	T	36	GENIC	homozygous	109962102
2	105065987	105065988	C	T	24	GENIC	homozygous	110580364
2	105066277	105066278	C	T	18	GENIC	homozygous	110580366
2	105067585	105067586	T	C	18	GENIC	homozygous	110580368
2	105068374	105068375	G	A	29	GENIC	homozygous	109962108
2	105069215	105069216	G	A	12	GENIC	homozygous	110580370
2	105069524	105069525	G	A	17	GENIC	homozygous	110580372
2	105070730	105070731	T	A	14	GENIC	homozygous	110580374
2	105072817	105072818	T	A	20	GENIC	homozygous	109962118
2	105073189	105073190	T	G	22	GENIC	homozygous	109962120
2	105074259	105074260	C	G	40	GENIC	homozygous	110580378
2	105074379	105074380	A	T	28	GENIC	homozygous	109962122
2	105074687	105074688	C	A	31	GENIC	homozygous	110580380
2	105076146	105076147	A	T	18	GENIC	homozygous	109962128
2	105078736	105078737	C	A	14	GENIC	homozygous	110580382
2	105080342	105080343	T	G	14	GENIC	homozygous	109962146
2	105081364	105081365	G	A	20	GENIC	homozygous	109962150
2	105081640	105081641	T	C	25	GENIC	homozygous	109962153
2	105082984	105082985	G	A	33	GENIC	homozygous	110580386
2	105083996	105083997	A	T	17	GENIC	homozygous	110580388
2	105084829	105084830	A	C	16	GENIC	homozygous	109962161
2	105085011	105085012	C	T	13	GENIC	possibly homozygous	110580390
2	105086231	105086232	G	A	35	GENIC	homozygous	109962163
2	105086240	105086241	A	G	33	GENIC	homozygous	109962164
2	105087444	105087445	C	T	19	GENIC	homozygous	110580394
2	105087578	105087579	C	A	19	GENIC	homozygous	109962176
2	105088266	105088267	T	C	27	GENIC	homozygous	110580396