chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	12716379	12716380	C	T	29	GENIC	homozygous	115362113
12	12717663	12717664	T	G	23	GENIC	possibly homozygous	115691201
12	12723132	12723133	A	G	8	GENIC	homozygous	115691204
12	12723237	12723238	T	G	34	GENIC	homozygous	115362115
12	12723324	12723325	A	T	22	GENIC	homozygous	115467271
12	12723668	12723669	C	T	34	GENIC	homozygous	115362116
12	12724578	12724579	C	T	27	GENIC	homozygous	115362117
12	12725525	12725526	G	C	19	GENIC	homozygous	115362118
12	12725607	12725608	T	C	16	GENIC	homozygous	115259025
12	12728200	12728201	A	G	32	GENIC	homozygous	115259035
12	12730351	12730352	C	G	19	GENIC	homozygous	115259049
12	12730829	12730830	A	G	25	GENIC	homozygous	115259051
12	12732488	12732489	A	G	16	GENIC	homozygous	115362119
12	12732633	12732634	T	A	20	GENIC	homozygous	115259059
12	12735082	12735083	C	T	29	GENIC	homozygous	115362120
12	12736236	12736237	G	A	32	GENIC	homozygous	115362122
12	12737654	12737655	T	A	35	GENIC	homozygous	115362123
12	12737834	12737835	C	A	32	GENIC	homozygous	115362124