chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	121829683	121829684	C	T	27	GENIC	homozygous	137606327
5	121829975	121829976	T		28	GENIC	homozygous	137337715
5	121832235	121832236	G	T	28	GENIC	homozygous	137606329
5	121836649	121836650	A	G	27	GENIC	homozygous	137606332
5	121837965	121837966	T	C	25	GENIC	homozygous	137606333
5	121831405	121831406	G	A	33	GENIC	homozygous	144739914
5	121832390	121832405	CCTCCCCCTGCAGAT		22	GENIC	homozygous	144701251
5	121839054	121839055	A	T	21	GENIC	homozygous	137606334
5	121840530	121840531	T	C	28	GENIC	homozygous	137606335
5	121844182	121844185	AAA		21	GENIC	homozygous	137337717
5	121844188	121844191	AAA		22	GENIC	homozygous	137337718