chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108774061887740619TC3GENIChomozygous68146157
108774072187740722AG2GENIChomozygous68146160
108774121587741216TC22GENIChomozygous68146162
108774184787741848TC16GENIChomozygous68146165
108774208987742090TG19GENIChomozygous68146168
108774241887742419GA24GENICpossibly homozygous68146171
108774372287743723TC8GENIChomozygous68146174
108774452487744525AG7GENIChomozygous68146177
108774491287744913GA15GENIChomozygous68146180
108774574187745742TC14GENIChomozygous68146183
108774639787746398TC15GENIChomozygous68146186
108774676987746770TC24GENIChomozygous68146189
108774808587748086CT17GENIChomozygous68146192
108774955887749559GC12GENIChomozygous68146198
108774960187749602GA11GENIChomozygous68146201
108775075487750755GA9GENIChomozygous68146204
108775099787750998CG7GENIChomozygous68146206
108775238387752384TA10GENIChomozygous68146209
108775246887752469TC9GENIChomozygous68146212