chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	113010120	113010121	T	C	19	GENIC	homozygous	109982630
2	113010264	113010265	C	T	25	GENIC	homozygous	120204260
2	113010422	113010423	T	A	25	GENIC	homozygous	109982631
2	113011656	113011657	T	C	23	GENIC	homozygous	109982632
2	113012204	113012205	A	G	21	GENIC	homozygous	109982633
2	113012640	113012641	T	C	3	GENIC	homozygous	109982635
2	113014029	113014030	A	G	17	GENIC	homozygous	109982638
2	113014267	113014268	C	T	26	GENIC	homozygous	109982639
2	113015298	113015299	A	G	28	GENIC	homozygous	109982641
2	113018390	113018391	G	A	33	GENIC	homozygous	120204261
2	113021355	113021356	A	G	34	GENIC	homozygous	109982646
2	113022692	113022693	G	A	26	GENIC	homozygous	109982647
2	113022868	113022869	C	T	13	GENIC	homozygous	109982648
2	113023140	113023141	G	A	18	GENIC	homozygous	109982649
2	113023211	113023212	C	T	12	GENIC	homozygous	109982650
2	113023379	113023380	C	T	10	GENIC	homozygous	109982651
2	113023733	113023734	G	A	10	GENIC	homozygous	109982663
2	113024552	113024553	G	A	23	GENIC	homozygous	109982664
2	113024826	113024827	A	G	22	GENIC	homozygous	109982665
2	113024887	113024888	G	T	20	GENIC	homozygous	109982666
2	113025390	113025391	T	A	15	GENIC	homozygous	109982668
2	113025583	113025584	C	T	18	GENIC	homozygous	120204262
2	113025706	113025707	C	T	22	GENIC	homozygous	109982669
2	113023528	113023529	G	T	2	GENIC	homozygous	120372322
2	113023529	113023530	G	T	2	GENIC	homozygous	120372323