chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	93656911	93656912	C	G	11	GENIC	homozygous	120144702
2	93657094	93657095	T	C	18	GENIC	homozygous	109920692
2	93657397	93657398	T	C	33	GENIC	homozygous	109920694
2	93658169	93658170	T	C	21	GENIC	homozygous	109920696
2	93658747	93658748	C	A	30	GENIC	homozygous	109920698
2	93659506	93659507	T	C	29	GENIC	homozygous	109920702
2	93659826	93659827	G	A	31	GENIC	homozygous	120125658
2	93660077	93660078	T	C	32	GENIC	homozygous	109920706
2	93660192	93660193	G	A	32	GENIC	homozygous	109920708
2	93660309	93660310	C	T	36	GENIC	homozygous	109920710
2	93660355	93660356	A	C	40	GENIC	homozygous	109920712
2	93660503	93660504	C	T	20	GENIC	homozygous	109920714
2	93660567	93660568	T	C	20	GENIC	homozygous	109920716
2	93661352	93661353	G	A	38	GENIC	homozygous	109920717
2	93662303	93662304	T	C	34	GENIC	homozygous	109920719
2	93663529	93663530	G	T	25	GENIC	homozygous	109920721
2	93663549	93663550	C	T	26	GENIC	homozygous	109920723
2	93664108	93664109	T	C	23	GENIC	homozygous	109920725
2	93664279	93664280	A	G	38	GENIC	homozygous	109920727
2	93664291	93664292	A	G	36	GENIC	homozygous	109920729
2	93664417	93664418	A	G	29	GENIC	homozygous	109920731
2	93664691	93664692	A	T	34	GENIC	homozygous	109920733
2	93665021	93665022	C	G	21	GENIC	homozygous	109920735
2	93665098	93665099	G	C	16	GENIC	homozygous	109920739
2	93665236	93665237	G	A	35	GENIC	homozygous	109920743
2	93665685	93665686	T	C	25	GENIC	homozygous	109920745
2	93665941	93665942	C	T	32	GENIC	homozygous	109920747