chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6118514057118514058TC25GENIChomozygous54961750
6118514886118514887CT33GENIChomozygous54961756
6118515159118515160TC36GENIChomozygous54961760
6118515311118515312AG27GENIChomozygous54961764
6118515678118515679TC32GENIChomozygous55265569
6118516392118516399TTTGTTG-------28GENIChomozygous54961770
6118516889118516890TC25GENIChomozygous54961774
6118517022118517025CCG---24GENIChomozygous55428873
6118517025118517026CCAA24GENIChomozygous55428875
6118517155118517156CA19GENIChomozygous54961776
6118517966118517967CCT2GENIChomozygous55265577
6118517979118517980CCG7GENIChomozygous55050799
6118518492118518493AT30GENIChomozygous54961782
6118519005118519006GA37GENIChomozygous55265580
6118520796118520797CT30GENIChomozygous55265583
6118520812118520813GA37GENIChomozygous55265586
6118521203118521204AG33GENIChomozygous54961804
6118522952118522953CT27GENIChomozygous55265589
6118524092118524093GC26GENIChomozygous55265591
6118524923118524924TC23GENIChomozygous54961818
6118527327118527328TTCACG10GENIChomozygous55265594
6118533368118533369AC15GENIChomozygous54961834
6118533591118533592AG15GENIChomozygous55265607
6118534284118534285TC31GENIChomozygous55265610
6118535312118535313GGTT7GENIChomozygous55428877
6118535319118535320GT7GENIChomozygous55428879
6118537606118537607TC19GENIChomozygous54961864
6118537854118537855CA29GENIChomozygous55265613
6118538632118538633GGA5GENICheterozygous55099022
6118536656118536657GGACACGCAC1GENIChomozygous55533195
6118538216118538222ACACAC------5GENICheterozygous55533197
6118538218118538222ACAC----5GENICheterozygous55533199
6118538942118538943TTA14GENICpossibly homozygous54961874