chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	18931346	18931347	C	T	16	GENIC	possibly homozygous	118247397
12	18931846	18931847	C	T	49	GENIC	homozygous	115277818
12	18931858	18931859	G	A	48	GENIC	homozygous	115277820
12	18931948	18931949	T	C	35	GENIC	homozygous	115277822
12	18932272	18932273	A	G	56	GENIC	homozygous	115277824
12	18932313	18932314	G	A	57	GENIC	homozygous	115277826
12	18933132	18933133	T	C	35	GENIC	homozygous	115277828
12	18934568	18934569	A	G	23	GENIC	heterozygous	118247398
12	18934897	18934898	C	T	48	GENIC	homozygous	115277830
12	18935719	18935720	A	T	45	GENIC	possibly homozygous	115277832
12	18936204	18936205	A	T	177	GENIC	heterozygous	118294769
12	18936206	18936207	C	T	180	GENIC	heterozygous	118247399
12	18936237	18936238	A	C	245	GENIC	heterozygous	118247400
12	18936249	18936250	C	T	101	GENIC	heterozygous	118294770
12	18936256	18936257	A	C	148	GENIC	heterozygous	118294771
12	18936283	18936284	T	C	91	GENIC	heterozygous	118294772
12	18936321	18936322	T	C	49	GENIC	homozygous	115277834
12	18936951	18936952	C	T	40	GENIC	possibly homozygous	115277836
12	18937123	18937124	T	C	201	GENIC	heterozygous	118294774
12	18937594	18937595	G	A	42	GENIC	homozygous	115277838
12	18938026	18938027	G	T	29	GENIC	heterozygous	118247402
12	18936228	18936229	T	C	247	GENIC	heterozygous	118336157
12	18934703	18934704	T	C	19	GENIC	homozygous	115365686