chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24091201	24091202	T	A	42	GENIC	homozygous	115286935
12	24091252	24091253	T	C	38	GENIC	possibly homozygous	115286937
12	24092899	24092900	C	G	26	GENIC	homozygous	115286951
12	24094587	24094588	C	T	42	GENIC	homozygous	115446303
12	24094788	24094789	G	A	32	GENIC	heterozygous	118337024
12	24094864	24094865	G	A	27	GENIC	heterozygous	118337025
12	24094974	24094975	A	T	31	GENIC	homozygous	118331636
12	24095109	24095110	G	T	29	GENIC	possibly homozygous	118324967
12	24095174	24095175	T	A	26	GENIC	possibly homozygous	118337026
12	24095442	24095443	C	A	40	GENIC	homozygous	115446305
12	24095500	24095501	G	A	41	GENIC	possibly homozygous	115446307
12	24095757	24095758	A	C	34	GENIC	homozygous	115438677
12	24097197	24097198	G	A	52	GENIC	homozygous	115446308
12	24097220	24097221	T	C	49	GENIC	homozygous	115446310
12	24097446	24097447	C	T	45	GENIC	homozygous	115446312
12	24098076	24098077	T	C	34	GENIC	homozygous	115438696
12	24099223	24099224	A	T	36	GENIC	homozygous	115438706
12	24099607	24099608	T	A	39	GENIC	homozygous	115438711
12	24101283	24101284	C	T	35	GENIC	possibly homozygous	115446318