chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	89180275	89180276	T	C	16	GENIC	homozygous	108884780
1	89180560	89180561	C	G	23	GENIC	homozygous	108884781
1	89180810	89180811	G	A	29	GENIC	homozygous	120780190
1	89185838	89185839	T	C	21	GENIC	homozygous	108884792
1	89185983	89185984	T	C	32	GENIC	homozygous	108884793
1	89186433	89186434	C	T	23	GENIC	homozygous	108884794
1	89187220	89187221	A	C	19	GENIC	homozygous	108884795
1	89187270	89187271	A	G	25	GENIC	homozygous	108884796
1	89188308	89188309	T	G	16	GENIC	homozygous	108884798
1	89188565	89188566	C	T	17	GENIC	homozygous	120780191
1	89189204	89189205	G	C	34	GENIC	homozygous	108884800
1	89187746	89187747	C	T	8	GENIC	homozygous	109308026
1	89187085	89187086	T	A	31	GENIC	homozygous	120483939
1	89187146	89187147	G	A	26	GENIC	homozygous	120483941
1	89192477	89192478	T	A	32	GENIC	homozygous	108884806
1	89192937	89192938	T	G	29	GENIC	homozygous	120780192
1	89193568	89193569	C	A	16	GENIC	homozygous	120780193