chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	84521871	84521872	T	C	24	GENIC	homozygous	109886629
2	84522929	84522930	A	G	16	GENIC	homozygous	109886631
2	84523701	84523702	G	C	23	GENIC	possibly homozygous	109886633
2	84524064	84524065	C	G	23	GENIC	homozygous	109886635
2	84524839	84524840	T	G	31	GENIC	homozygous	110945975
2	84525150	84525151	T	C	30	GENIC	homozygous	109886638
2	84525549	84525550	A	G	35	GENIC	homozygous	110945977
2	84525715	84525716	A	C	22	GENIC	homozygous	110945979
2	84525722	84525723	C	T	24	GENIC	homozygous	110945981
2	84525759	84525760	G	C	32	GENIC	homozygous	109886642
2	84525840	84525841	C	T	27	GENIC	homozygous	110945983
2	84526083	84526084	T	A	26	GENIC	homozygous	110945985
2	84526838	84526839	C	T	38	GENIC	homozygous	110945991
2	84528078	84528079	T	C	24	GENIC	homozygous	109886649
2	84529130	84529131	A	G	11	GENIC	homozygous	110945999
2	84529208	84529209	A	G	19	GENIC	homozygous	110946001
2	84529599	84529600	G	A	22	GENIC	homozygous	110946003
2	84529972	84529973	T	C	12	GENIC	homozygous	110946005
2	84529976	84529977	T	C	12	GENIC	homozygous	110946007
2	84529988	84529989	G	A	10	GENIC	homozygous	110946009
2	84530106	84530107	C	T	32	GENIC	homozygous	110946013
2	84530802	84530803	G	A	17	GENIC	homozygous	110946017