chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X123900994123900995AG16GENIChomozygous992484257
X123901333123901334TC17GENIChomozygous992484258
X123901666123901667CA13GENIChomozygous992484259
X123902771123902772CT21GENIChomozygous992484260
X123903040123903041CT25GENIChomozygous992484261
X123903719123903720TA17GENIChomozygous992484262
X123904966123904967GA18GENIChomozygous992484263
X123905627123905628AG18GENIChomozygous992484264
X123906352123906353GT10GENIChomozygous992484265
X123906808123906809AG17GENIChomozygous992484266
X123906932123906933TA25GENIChomozygous992484267
X123907599123907600CT18GENIChomozygous992484268
X123909136123909137CG20GENIChomozygous992484269
X123911321123911322TC11INTERGENIChomozygous992484270
X123911461123911462GT19INTERGENIChomozygous992484271
X123911482123911483GA21INTERGENIChomozygous992484272
X123911483123911484TG21INTERGENIChomozygous992484273
X123912197123912198TC23INTERGENIChomozygous992484274
X123914613123914614AG20INTERGENIChomozygous992484275
X123916196123916197AG23INTERGENIChomozygous992484276
X123916552123916553GA18INTERGENIChomozygous992484277
X123916936123916937AG22INTERGENIChomozygous992484278