chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	113009946	113009947	T	G	11	GENIC	homozygous	109982627
2	113010120	113010121	T	C	14	GENIC	homozygous	109982630
2	113010422	113010423	T	A	23	GENIC	homozygous	109982631
2	113011656	113011657	T	C	31	GENIC	homozygous	109982632
2	113012204	113012205	A	G	20	GENIC	homozygous	109982633
2	113012406	113012407	G	A	18	GENIC	homozygous	109982634
2	113013558	113013559	A	G	31	GENIC	homozygous	109982637
2	113014029	113014030	A	G	22	GENIC	homozygous	109982638
2	113014267	113014268	C	T	17	GENIC	homozygous	109982639
2	113014293	113014294	A	T	20	GENIC	homozygous	109982640
2	113015298	113015299	A	G	36	GENIC	possibly homozygous	109982641
2	113015945	113015946	G	T	20	GENIC	homozygous	109982642
2	113019087	113019088	C	A	30	GENIC	homozygous	109982643
2	113019268	113019269	G	T	29	GENIC	homozygous	109982644
2	113019763	113019764	C	T	11	GENIC	homozygous	109982645
2	113021355	113021356	A	G	39	GENIC	homozygous	109982646
2	113022692	113022693	G	A	32	GENIC	homozygous	109982647
2	113022868	113022869	C	T	24	GENIC	homozygous	109982648
2	113023140	113023141	G	A	17	GENIC	homozygous	109982649
2	113023211	113023212	C	T	7	GENIC	homozygous	109982650
2	113023379	113023380	C	T	10	GENIC	homozygous	109982651
2	113023485	113023486	C	A	11	GENIC	homozygous	109982659
2	113023490	113023491	C	T	11	GENIC	homozygous	109982660
2	113023733	113023734	G	A	18	GENIC	homozygous	109982663
2	113024552	113024553	G	A	27	GENIC	homozygous	109982664
2	113024826	113024827	A	G	29	GENIC	homozygous	109982665
2	113024887	113024888	G	T	27	GENIC	homozygous	109982666
2	113025108	113025109	G	A	24	GENIC	homozygous	109982667
2	113025390	113025391	T	A	20	GENIC	possibly homozygous	109982668
2	113025706	113025707	C	T	29	GENIC	homozygous	109982669