chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	47922519	47922520	C	A	15	GENIC	homozygous	118272882
12	47922782	47922783	C	T	50	GENIC	homozygous	115444256
12	47923004	47923005	A	G	23	GENIC	homozygous	118272883
12	47923026	47923027	G	T	15	GENIC	homozygous	118272884
12	47923075	47923076	A	T	8	GENIC	heterozygous	118272885
12	47923658	47923659	T	C	16	GENIC	heterozygous	118379614
12	47923662	47923663	T	C	18	GENIC	heterozygous	118333840
12	47923754	47923755	T	G	24	GENIC	homozygous	118306267
12	47923824	47923825	G	T	33	GENIC	possibly homozygous	118272886
12	47923864	47923865	T	C	33	GENIC	heterozygous	118272887
12	47924124	47924125	C	T	8	GENIC	homozygous	115345054
12	47924700	47924701	T	C	28	GENIC	homozygous	115345060
12	47925068	47925069	A	G	33	GENIC	homozygous	115345062
12	47926940	47926941	A	C	27	GENIC	homozygous	115345064
12	47926976	47926977	T	C	32	GENIC	homozygous	115345066
12	47927666	47927667	A	G	44	GENIC	homozygous	115345068
12	47927790	47927791	A	G	49	GENIC	homozygous	115345074
12	47928117	47928118	T	C	32	GENIC	homozygous	115345076
12	47930417	47930418	A	G	29	GENIC	homozygous	115345078
12	47931564	47931565	A	G	38	GENIC	homozygous	115345080
12	47932812	47932813	A	G	11	GENIC	homozygous	115398653
12	47934691	47934692	T	G	16	GENIC	homozygous	115622623