chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6118514057118514058TC32GENIChomozygous54961750
6118514886118514887CT29GENIChomozygous54961756
6118515159118515160TC19GENIChomozygous54961760
6118515311118515312AG27GENIChomozygous54961764
6118515678118515679TC31GENIChomozygous55265569
6118516392118516399TTTGTTG-------38GENIChomozygous54961770
6118516889118516890TC35GENIChomozygous54961774
6118517022118517025CCG---30GENIChomozygous55428873
6118517025118517026CCAA30GENIChomozygous55428875
6118517155118517156CA34GENIChomozygous54961776
6118517966118517967CCT4GENIChomozygous55265577
6118517979118517980CCG10GENIChomozygous55050799
6118518492118518493AT29GENIChomozygous54961782
6118519005118519006GA33GENIChomozygous55265580
6118520796118520797CT26GENIChomozygous55265583
6118520812118520813GA28GENIChomozygous55265586
6118521203118521204AG27GENIChomozygous54961804
6118522952118522953CT16GENIChomozygous55265589
6118524092118524093GC21GENIChomozygous55265591
6118524923118524924TC33GENIChomozygous54961818
6118533368118533369AC17GENIChomozygous54961834
6118533591118533592AG27GENIChomozygous55265607
6118534284118534285TC29GENIChomozygous55265610
6118535312118535313GGTT10GENIChomozygous55428877
6118535319118535320GT10GENIChomozygous55428879
6118537606118537607TC36GENIChomozygous54961864
6118537854118537855CA29GENIChomozygous55265613
6118538218118538222ACAC----1GENIChomozygous55533199
6118536656118536657GGACACGCAC3GENICheterozygous55533195
6118538942118538943TTA17GENIChomozygous54961874