chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109128948	109128949	A	C	21	GENIC	homozygous	51773193
10	109129155	109129156	G	A	20	GENIC	homozygous	51598622
10	109129272	109129273	T	C	28	GENIC	homozygous	51598623
10	109129839	109129840	G	A	13	GENIC	homozygous	51955671
10	109130256	109130257	A	G	29	GENIC	possibly homozygous	51598626
10	109130337	109130340	AGT	---	8	GENIC	heterozygous	51598627
10	109130366	109130367	G	A	22	GENIC	possibly homozygous	51598628
10	109130415	109130416	C	G	17	GENIC	homozygous	51598629
10	109130508	109130509	T	G	24	GENIC	homozygous	51598630
10	109130539	109130541	TG	--	10	GENIC	possibly homozygous	51955674
10	109131102	109131103	G	GTTGTT	3	GENIC	homozygous	51598635
10	109134268	109134269	G	A	11	GENIC	possibly homozygous	51955680
10	109134510	109134511	G	A	23	GENIC	homozygous	51955683