chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18012738980127390TG32GENIChomozygous109298243
18013076880130769TG34GENIChomozygous109298245
18013079280130793TG31GENIChomozygous109298247
18013079680130797TG35GENICheterozygous109298249
18013108680131087AG37GENIChomozygous109298251
18013131180131312GA34GENIChomozygous109298253
18013152380131524CA13GENIChomozygous109298255
18013266880132669CT20GENICpossibly homozygous109298257
18013268280132683GA16GENICheterozygous109298259
18013268980132690CG16GENICheterozygous109298261
18013277480132775CT2GENIChomozygous109298263
18013279280132793TC7GENIChomozygous109298265
18013282380132824GT20GENIChomozygous109298267
18013282780132828CT20GENIChomozygous109298269