chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	84520712	84520713	C	T	32	GENIC	homozygous	120301389
2	84523075	84523076	A	G	35	GENIC	homozygous	120301390
2	84523251	84523252	A	C	37	GENIC	homozygous	120301391
2	84524064	84524065	C	G	24	GENIC	homozygous	109886635
2	84521871	84521872	T	C	28	GENIC	homozygous	109886629
2	84523701	84523702	G	C	27	GENIC	homozygous	109886633
2	84524839	84524840	T	G	38	GENIC	homozygous	110945975
2	84524877	84524878	T	G	33	GENIC	homozygous	120301392
2	84525021	84525022	G	A	30	GENIC	homozygous	120301393
2	84525150	84525151	T	C	37	GENIC	homozygous	109886638
2	84525302	84525303	C	T	42	GENIC	homozygous	120301394
2	84525549	84525550	A	G	30	GENIC	homozygous	110945977
2	84525715	84525716	A	C	27	GENIC	homozygous	110945979
2	84525722	84525723	C	T	26	GENIC	homozygous	110945981
2	84525759	84525760	G	C	25	GENIC	homozygous	109886642
2	84525877	84525878	C	A	25	GENIC	homozygous	120301395
2	84526083	84526084	T	A	22	GENIC	homozygous	110945985
2	84528078	84528079	T	C	17	GENIC	homozygous	109886649
2	84528692	84528693	C	T	23	GENIC	homozygous	120301396
2	84529208	84529209	A	G	11	GENIC	homozygous	110946001
2	84529598	84529599	C	T	29	GENIC	homozygous	120301397
2	84529972	84529973	T	C	20	GENIC	homozygous	110946005
2	84529976	84529977	T	C	20	GENIC	homozygous	110946007
2	84529988	84529989	G	A	26	GENIC	homozygous	110946009