chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40511610	40511611	C	T	12	GENIC	homozygous	115383859
12	40516305	40516306	G	A	11	GENIC	homozygous	115328332
12	40516663	40516664	A	G	19	GENIC	homozygous	115328334
12	40519011	40519012	C	G	25	GENIC	homozygous	115383867
12	40520601	40520602	G	A	20	GENIC	homozygous	115383869
12	40521940	40521941	G	C	20	GENIC	homozygous	115328340
12	40518792	40518793	C	T	19	GENIC	homozygous	115328336
12	40518867	40518868	A	C	21	GENIC	homozygous	115328338
12	40524911	40524912	C	T	19	GENIC	homozygous	115328342
12	40526616	40526617	A	G	21	GENIC	homozygous	115328344
12	40527560	40527561	T	G	5	GENIC	homozygous	115328346