chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	16016223	16016224	T	C	36	GENIC	homozygous	115468643
12	16016314	16016315	C	T	31	GENIC	homozygous	115468645
12	16016437	16016438	A	G	24	GENIC	homozygous	115468647
12	16017273	16017274	T	C	22	GENIC	homozygous	115468649
12	16017402	16017403	G	A	33	GENIC	homozygous	115468651
12	16017411	16017412	T	C	24	GENIC	homozygous	115468653
12	16017636	16017637	G	A	37	GENIC	homozygous	115468655
12	16017724	16017725	C	G	32	GENIC	homozygous	115468657
12	16017771	16017772	G	A	28	GENIC	homozygous	115468659
12	16018768	16018769	T	A	21	GENIC	homozygous	115468661
12	16018788	16018789	G	A	23	GENIC	homozygous	115468663
12	16018885	16018886	T	C	33	GENIC	homozygous	115468665
12	16019200	16019201	T	C	24	GENIC	homozygous	115468667
12	16019834	16019835	C	T	32	GENIC	homozygous	115468669
12	16020555	16020556	C	T	22	GENIC	homozygous	115468671
12	16020626	16020627	G	A	20	GENIC	homozygous	115468673
12	16020782	16020783	G	A	16	GENIC	homozygous	115468675
12	16020790	16020791	G	A	20	GENIC	homozygous	115468677
12	16020806	16020807	A	G	28	GENIC	homozygous	115468679
12	16020970	16020971	C	T	34	GENIC	homozygous	115468681
12	16021740	16021741	G	T	28	GENIC	homozygous	115468683
12	16022727	16022728	A	G	11	GENIC	homozygous	115269037
12	16023400	16023401	C	T	40	GENIC	homozygous	115468685
12	16023464	16023465	C	T	34	GENIC	homozygous	115269039
12	16023569	16023570	T	C	24	GENIC	homozygous	115468687
12	16023574	16023575	G	A	23	GENIC	homozygous	115468689
12	16023875	16023876	T	C	30	GENIC	homozygous	115468691
12	16023906	16023907	G	T	36	GENIC	homozygous	115468693
12	16024922	16024923	T	C	21	GENIC	homozygous	115468695
12	16025021	16025022	A	C	24	GENIC	homozygous	115468697
12	16025963	16025964	A	C	39	GENIC	homozygous	115269043
12	16028421	16028422	A	G	18	GENIC	homozygous	115420971