chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	84520935	84520936	A	C	14	GENIC	homozygous	109886628
2	84521634	84521635	G	A	46	GENIC	homozygous	110945971
2	84524285	84524286	G	A	36	GENIC	homozygous	110945973
2	84524839	84524840	T	G	39	GENIC	homozygous	110945975
2	84525150	84525151	T	C	29	GENIC	homozygous	109886638
2	84525549	84525550	A	G	50	GENIC	homozygous	110945977
2	84525715	84525716	A	C	30	GENIC	homozygous	110945979
2	84525722	84525723	C	T	30	GENIC	homozygous	110945981
2	84525759	84525760	G	C	40	GENIC	homozygous	109886642
2	84525840	84525841	C	T	42	GENIC	possibly homozygous	110945983
2	84526083	84526084	T	A	34	GENIC	homozygous	110945985
2	84526166	84526167	G	A	45	GENIC	homozygous	110945987
2	84526599	84526600	G	A	43	GENIC	homozygous	109886645
2	84526621	84526622	G	A	62	GENIC	heterozygous	110945989
2	84526838	84526839	C	T	42	GENIC	homozygous	110945991
2	84527146	84527147	C	A	29	GENIC	homozygous	110945993
2	84527916	84527917	T	A	8	GENIC	heterozygous	110945995
2	84527918	84527919	G	A	8	GENIC	heterozygous	110945997
2	84528078	84528079	T	C	27	GENIC	homozygous	109886649
2	84529130	84529131	A	G	20	GENIC	homozygous	110945999
2	84529208	84529209	A	G	42	GENIC	homozygous	110946001
2	84529599	84529600	G	A	26	GENIC	possibly homozygous	110946003
2	84529972	84529973	T	C	38	GENIC	homozygous	110946005
2	84529976	84529977	T	C	39	GENIC	homozygous	110946007
2	84529988	84529989	G	A	39	GENIC	homozygous	110946009
2	84530088	84530089	G	A	55	GENIC	homozygous	110946011
2	84530106	84530107	C	T	57	GENIC	homozygous	110946013
2	84530483	84530484	G	A	27	GENIC	homozygous	110946015
2	84530802	84530803	G	A	34	GENIC	homozygous	110946017
2	84530986	84530987	C	G	34	GENIC	homozygous	110946019