chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117492868874928689CT15GENICpossibly homozygous141038862
117492870874928709C14GENIChomozygous403310367
117492870874928709CA14GENICheterozygous403310368
117492871074928711C14GENIChomozygous403310369
117492871074928711CA14GENICheterozygous403310370
117492871074928711CT14GENICheterozygous403310371
117493756674937566T12GENIChomozygous138895607
117493756774937568AG12GENICheterozygous403310372
117493756774937568A12GENIChomozygous403310373
117493756974937570AG12GENICheterozygous403310374
117493756974937570A12GENIChomozygous403310375
117500254675002547G9GENICheterozygous403310387
117500254675002547GT9GENIChomozygous403310388
117500255775002558TG9GENIChomozygous141038865