chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	119734939	119734940	C	T	66	GENIC	possibly homozygous	54082127
7	119735737	119735738	A	G	74	GENIC	homozygous	54082128
7	119737142	119737143	C	T	67	GENIC	homozygous	54082129
7	119737538	119737539	A	G	42	GENIC	homozygous	54082130
7	119738820	119738821	G	A	58	GENIC	homozygous	54082131
7	119739193	119739194	G	A	61	GENIC	homozygous	54082132
7	119740085	119740086	T	C	39	GENIC	possibly homozygous	54082133
7	119740147	119740148	C	T	33	GENIC	heterozygous	54082134
7	119740170	119740171	G	A	38	GENIC	heterozygous	54233069
7	119740189	119740190	C	T	37	GENIC	heterozygous	54082135
7	119740285	119740286	C	G	40	GENIC	heterozygous	54233071
7	119740501	119740502	G	A	44	GENIC	possibly homozygous	54082136
7	119741029	119741030	T	TG	30	GENIC	possibly homozygous	54082137
7	119741029	119741030	T	TGTG	30	GENIC	heterozygous	54233073
7	119741030	119741031	G	GT	34	GENIC	homozygous	54082138