chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	107355834	107355835	T	C	78	GENIC	heterozygous	113955543
5	107355864	107355865	G	A	83	GENIC	heterozygous	113955544
5	107355888	107355889	G	A	73	GENIC	heterozygous	113955545
5	107355904	107355905	G	A	70	GENIC	heterozygous	113955546
5	107355927	107355928	C	G	73	GENIC	heterozygous	113955547
5	107355931	107355932	G	A	74	GENIC	heterozygous	113955548
5	107355941	107355942	G	T	69	GENIC	heterozygous	113955549
5	107355942	107355943	G	T	67	GENIC	heterozygous	113955550
5	107355953	107355954	T	C	59	GENIC	heterozygous	113955551
5	107355959	107355960	C	T	54	GENIC	heterozygous	113955552
5	107355961	107355962	A	C	51	GENIC	heterozygous	113955553
5	107355963	107355964	G	A	51	GENIC	heterozygous	113955554
5	107355990	107355991	G	C	54	GENIC	heterozygous	113955555
5	107355998	107355999	G	A	54	GENIC	heterozygous	113955556
5	107356013	107356014	C	T	44	GENIC	heterozygous	113955557
5	107356015	107356016	G	A	43	GENIC	heterozygous	113955558
5	107356023	107356024	G	A	42	GENIC	heterozygous	113955559
5	107356030	107356031	A	G	33	GENIC	heterozygous	113955560
5	107356058	107356059	C	A	44	GENIC	heterozygous	113955561
5	107356073	107356074	G	A	34	GENIC	heterozygous	113955562
5	107356074	107356075	C	T	34	GENIC	heterozygous	113955563