chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	31867620	31867621	G	A	30	GENIC	homozygous	111781433
16	31867621	31867622	A	G	30	GENIC	homozygous	111781435
16	31938574	31938575	A	C	49	GENIC	homozygous	112055635
16	31939079	31939080	T	G	22	GENIC	homozygous	112055636
16	31939492	31939493	T	C	28	GENIC	homozygous	112055637
16	31940901	31940902	G	A	23	GENIC	homozygous	112055638
16	31941327	31941328	A	G	19	GENIC	homozygous	112055639
16	31942588	31942589	G	T	33	GENIC	homozygous	112055640
16	31944667	31944668	A	G	33	GENIC	homozygous	112055641
16	31945259	31945260	A	G	25	GENIC	homozygous	112055642
16	31945378	31945379	T	G	20	GENIC	homozygous	112055643
16	31946253	31946254	T	A	31	GENIC	possibly homozygous	112055644
16	31946635	31946636	C	T	41	GENIC	homozygous	112055645
16	31946875	31946876	A	G	30	GENIC	homozygous	112055646
16	31947272	31947273	A	G	36	GENIC	homozygous	112055647
16	31947582	31947583	T	A	21	GENIC	homozygous	112055648
16	31948134	31948135	A	G	17	GENIC	homozygous	112055649