chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	19058564	19058565	G	T	22	GENIC	homozygous	111176121
17	19059762	19059763	C	T	28	GENIC	homozygous	111296823
17	19060173	19060174	T	A	37	GENIC	homozygous	111176125
17	19060506	19060507	T	C	33	GENIC	possibly homozygous	111296824
17	19060541	19060542	C	T	39	GENIC	possibly homozygous	111296825
17	19061249	19061250	A	G	22	GENIC	homozygous	111176129
17	19061570	19061571	C	T	21	GENIC	homozygous	111296826
17	19061968	19061969	T	C	19	GENIC	homozygous	111176139
17	19062322	19062323	A	G	23	GENIC	homozygous	111176141
17	19062499	19062500	G	A	15	GENIC	homozygous	111176143
17	19062898	19062899	A	G	23	GENIC	homozygous	111176147