chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	62569788	62569789	G	A	31	GENIC	homozygous	118147138
8	62571018	62571019	A	G	20	GENIC	homozygous	116836899
8	62576079	62576080	G	A	16	GENIC	possibly homozygous	116836917
8	62582478	62582479	C	T	34	GENIC	homozygous	116836943
8	62584192	62584193	A	G	42	GENIC	homozygous	116836949
8	62584296	62584297	T	C	19	GENIC	homozygous	116836951
8	62586659	62586660	C	G	17	GENIC	homozygous	116836957
8	62587592	62587593	A	T	32	GENIC	homozygous	116836963
8	62590305	62590306	G	A	24	GENIC	homozygous	118147141
8	62590871	62590872	G	A	25	GENIC	homozygous	118147143
8	62595352	62595353	A	G	32	GENIC	homozygous	116836985
8	62597866	62597867	G	A	25	GENIC	homozygous	118147145
8	62599112	62599113	G	A	22	GENIC	homozygous	118147147
8	62597878	62597879	A	T	28	GENIC	homozygous	116836993
8	62607632	62607633	A	C	36	GENIC	homozygous	118147149
8	62609830	62609831	A	G	36	GENIC	homozygous	116837027
8	62610865	62610866	G	A	22	GENIC	homozygous	118147151
8	62613961	62613962	G	A	12	GENIC	homozygous	118147153
8	62614517	62614518	G	A	28	GENIC	homozygous	118147155
8	62614792	62614793	T	G	35	GENIC	homozygous	116837037
8	62616043	62616044	T	C	27	GENIC	homozygous	116837039
8	62616558	62616559	C	T	7	GENIC	homozygous	116837041