chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2232903106232903107CT20GENICpossibly homozygous74941059
2232903116232903117CT20GENICpossibly homozygous75311452
2232904010232904011CT15GENIChomozygous75311453
2232904653232904654AG7GENIChomozygous74451029
2232905340232905341TC20GENIChomozygous74451033
2232905989232905990TC25GENIChomozygous74451035
2232906622232906623GT19GENICpossibly homozygous75311455
2232906645232906646TC15GENICpossibly homozygous75311456
2232913111232913112TC33GENIChomozygous74451045
2232913191232913192CT20GENIChomozygous75311457
2232913249232913250GA19GENIChomozygous75311458
2232913275232913276GT18GENIChomozygous74451047
2232913331232913332CT14GENIChomozygous75311459
2232913522232913523CG37GENIChomozygous75311460
2232913560232913561CG40GENIChomozygous74451049
2232913830232913831GA16GENICpossibly homozygous74451051
2232914588232914589CT31GENIChomozygous75311461
2232915524232915525GA24GENIChomozygous75311462
2232916143232916144CT4GENIChomozygous75311463
2232917271232917272GA16GENIChomozygous74451059
2232917559232917560TC42GENIChomozygous74451061
2232918789232918790AG27GENIChomozygous74451063
2232920014232920015AG34GENIChomozygous74451069
2232920161232920162TG22GENIChomozygous74451071
2232920885232920886GC22GENICpossibly homozygous75311466
2232921234232921235GA40GENIChomozygous75311467
2232921637232921638GT40GENIChomozygous75857846
2232921638232921639GC40GENIChomozygous74451079
2232921959232921960AG11GENIChomozygous75311468
2232923129232923130CG17GENICheterozygous74451085
2232924072232924073CA13GENIChomozygous74451087
2232926033232926034AG19GENIChomozygous74451093
2232926253232926254AC19GENIChomozygous75311469
2232926760232926761CT13GENIChomozygous75311470
2232927176232927177GA28GENIChomozygous74451095
2232927326232927327CT27GENIChomozygous75311471