chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39302956	39302957	C	T	42	GENIC	homozygous	139141947
12	39304574	39304575	G	A	45	GENIC	homozygous	139141950
12	39305069	39305070	C	T	27	GENIC	homozygous	142340400
12	39305441	39305442	C	A	49	GENIC	homozygous	139141953
12	39305553	39305554	A	G	57	GENIC	homozygous	139141954
12	39305583	39305584	T	C	54	GENIC	homozygous	139141955
12	39305776	39305777	C	A	66	GENIC	possibly homozygous	142340401
12	39305964	39305965	T	C	45	GENIC	homozygous	139141956
12	39306623	39306624	T	C	46	GENIC	homozygous	139141957
12	39307001	39307002	G	A	54	GENIC	homozygous	139141958