chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	61759961	61759962	A	T	3	GENIC	heterozygous	112356108
16	61760278	61760279	G	A	25	GENIC	homozygous	112356110
16	61760816	61760817	T	C	20	GENIC	homozygous	112356112
16	61761853	61761854	G	A	7	GENIC	homozygous	112167270
16	61761868	61761869	C	T	7	GENIC	homozygous	112008298
16	61763006	61763007	A	G	18	GENIC	homozygous	112167272
16	61763302	61763303	C	G	15	GENIC	homozygous	112167274
16	61763857	61763858	T	C	22	GENIC	homozygous	112167276
16	61764489	61764490	C	A	15	GENIC	homozygous	112356114
16	61764725	61764726	A	T	19	GENIC	homozygous	112167278
16	61764886	61764887	A	G	7	GENIC	heterozygous	125736640
16	61765034	61765035	T	C	10	GENIC	homozygous	112008306
16	61765785	61765786	A	G	15	GENIC	homozygous	112167280
16	61767047	61767048	A	G	18	GENIC	homozygous	112008312
16	61767319	61767320	G	A	22	GENIC	homozygous	112167282
16	61767647	61767648	C	A	14	GENIC	homozygous	112008316
16	61767789	61767790	G	A	15	GENIC	homozygous	112008318
16	61767815	61767816	G	A	18	GENIC	homozygous	112167284
16	61768477	61768478	G	A	13	GENIC	homozygous	112167286
16	61768729	61768730	C	T	18	GENIC	homozygous	112167292
16	61769076	61769077	G	A	10	GENIC	homozygous	112167294