chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109129155	109129156	G	A	23	GENIC	possibly homozygous	51598622
10	109129272	109129273	T	C	18	GENIC	homozygous	51598623
10	109129769	109129770	C	T	15	GENIC	possibly homozygous	51598625
10	109130256	109130257	A	G	22	GENIC	homozygous	51598626
10	109130337	109130340	AGT	---	11	GENIC	possibly homozygous	51598627
10	109130366	109130367	G	A	15	GENIC	possibly homozygous	51598628
10	109130415	109130416	C	G	33	GENIC	possibly homozygous	51598629
10	109130508	109130509	T	G	32	GENIC	homozygous	51598630
10	109130537	109130541	TGTG	----	10	GENIC	homozygous	51598631
10	109130886	109130887	A	AGTGTGT	1	GENIC	homozygous	51598632
10	109131102	109131103	G	GTTGTT	5	GENIC	homozygous	51598635
10	109134036	109134037	G	C	30	GENIC	homozygous	51598638