chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	10729115	10729116	A	C	14	GENIC	homozygous	111724252
16	10729649	10729650	G	C	19	GENIC	homozygous	111934015
16	10729668	10729669	G	A	21	GENIC	homozygous	111934017
16	10730137	10730138	A	G	19	GENIC	homozygous	111934019
16	10730143	10730144	G	A	19	GENIC	homozygous	111934021
16	10730830	10730831	C	A	18	GENIC	homozygous	111724256
16	10731240	10731241	C	G	24	GENIC	heterozygous	119191377
16	10731268	10731269	C	G	22	GENIC	possibly homozygous	119142516
16	10732737	10732738	A	G	19	GENIC	homozygous	111724258
16	10733647	10733648	T	C	11	GENIC	homozygous	111934023
16	10734593	10734594	T	G	11	GENIC	homozygous	111724260
16	10735028	10735029	G	A	15	GENIC	homozygous	111724264
16	10739146	10739147	C	A	20	GENIC	homozygous	119191378
16	10742466	10742467	C	T	19	GENIC	homozygous	111934025
16	10743367	10743368	A	G	22	GENIC	homozygous	111934027
16	10743632	10743633	G	A	19	GENIC	homozygous	111934029
16	10743819	10743820	C	G	22	GENIC	homozygous	111934031
16	10744209	10744210	G	T	24	GENIC	possibly homozygous	111934033
16	10745507	10745508	G	A	24	GENIC	homozygous	111934035
16	10745638	10745639	C	T	25	GENIC	homozygous	111934037
16	10746275	10746276	T	A	21	GENIC	homozygous	111934039
16	10747620	10747621	G	A	27	GENIC	homozygous	111934041
16	10747791	10747792	C	T	28	GENIC	homozygous	111934043
16	10748629	10748630	T	C	21	GENIC	homozygous	111934045
16	10749215	10749216	T	C	22	GENIC	homozygous	111934047