chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6118514057118514058TC24GENIChomozygous54961750
6118514886118514887CT25GENIChomozygous54961756
6118515159118515160TC35GENIChomozygous54961760
6118515311118515312AG34GENIChomozygous54961764
6118515678118515679TC32GENIChomozygous55265569
6118516392118516399TTTGTTG-------35GENIChomozygous54961770
6118516889118516890TC30GENIChomozygous54961774
6118517155118517156CA39GENIChomozygous54961776
6118517966118517967CCT12GENICheterozygous55265577
6118517979118517980CCG16GENIChomozygous55050799
6118518492118518493AT30GENIChomozygous54961782
6118519005118519006GA38GENIChomozygous55265580
6118520796118520797CT47GENIChomozygous55265583
6118520812118520813GA46GENIChomozygous55265586
6118521203118521204AG39GENICpossibly homozygous54961804
6118522952118522953CT32GENIChomozygous55265589
6118524092118524093GC30GENIChomozygous55265591
6118524923118524924TC29GENIChomozygous54961818
6118527327118527328TTCACG7GENIChomozygous55265594
6118517022118517025CCG---41GENIChomozygous55428873
6118517025118517026CCAA40GENIChomozygous55428875
6118528257118528258CCGTCTGTTT8GENICheterozygous55612863
6118533368118533369AC15GENIChomozygous54961834
6118533591118533592AG23GENIChomozygous55265607
6118534284118534285TC24GENIChomozygous55265610
6118535312118535313GGTT7GENIChomozygous55428877
6118535319118535320GT7GENIChomozygous55428879
6118537606118537607TC36GENIChomozygous54961864
6118537854118537855CA31GENIChomozygous55265613
6118538632118538633GGA2GENIChomozygous55099022
6118538942118538943TTA24GENICpossibly homozygous54961874
6118538218118538222ACAC----5GENICheterozygous55533199
6118536656118536657GGACACGCAC2GENIChomozygous55533195
6118538216118538222ACACAC------5GENICheterozygous55533197