chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	123210480	123210481	G	T	57	GENIC	homozygous	111692078
3	123210509	123210510	A	G	53	GENIC	homozygous	111692079
3	123210663	123210664	A	T	33	GENIC	homozygous	111692080
3	123211679	123211680	T	C	51	GENIC	possibly homozygous	111692081
3	123212764	123212765	C	T	29	GENIC	homozygous	111692082
3	123213093	123213094	G	A	54	GENIC	possibly homozygous	111692083
3	123213309	123213310	C	T	41	GENIC	homozygous	111692084
3	123213588	123213589	T	A	50	GENIC	homozygous	111692085
3	123214018	123214019	T	G	48	GENIC	homozygous	111692086
3	123214646	123214647	C	T	61	GENIC	homozygous	111692087
3	123215525	123215526	A	T	55	GENIC	homozygous	111692088
3	123215919	123215920	A	G	42	GENIC	homozygous	111692089
3	123216926	123216927	G	A	71	GENIC	possibly homozygous	111692090
3	123217142	123217143	A	G	34	GENIC	homozygous	111692091
3	123217390	123217391	C	T	54	GENIC	homozygous	111692092
3	123217471	123217472	G	A	52	GENIC	homozygous	111692093
3	123219865	123219866	C	T	32	GENIC	homozygous	111692094