chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5143111826143111827AG34GENIChomozygous114034270
5143111845143111846TA30GENIChomozygous114034271
5143112759143112760CT20GENIChomozygous114034272
5143112970143112971TC20GENIChomozygous114034273
5143113027143113028AG19GENIChomozygous114034274
5143113032143113033CT18GENIChomozygous114034275
5143115595143115596CA9GENIChomozygous114034278
5143115597143115598CT9GENIChomozygous114034279
5143115608143115609AC9GENIChomozygous114034280
5143115666143115667CG21GENIChomozygous114034281
5143115672143115673CG20GENIChomozygous114034282
5143115688143115689CA18GENIChomozygous114034283
5143115706143115707CG21GENIChomozygous114034284
5143115933143115934AG23GENIChomozygous114034285
5143116126143116127GA24GENIChomozygous114034286
5143116651143116652CA39GENIChomozygous114034287
5143116675143116676TC36GENIChomozygous114034288
5143116751143116752TG40GENIChomozygous114034289
5143117306143117307AG37GENIChomozygous114034290
5143118472143118473CT24GENIChomozygous114034291
5143119414143119415TA36GENIChomozygous114034292