chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4107135297107135298GA39GENICheterozygous113151003
4107135298107135299TC40GENICheterozygous113151004
4107135314107135315TC36GENICheterozygous113151005
4107135352107135353CT42GENICheterozygous112806320
4107135390107135391TC41GENICheterozygous112806322
4107135467107135468CT39GENICheterozygous113046550
4107135525107135526CT33GENICheterozygous113151006
4107137082107137083CT56GENICheterozygous112806330
4107137165107137166CA57GENICheterozygous113151007
4107137213107137214TG49GENICheterozygous112806332
4107137235107137236GA47GENICheterozygous112806334
4107137350107137351AC19GENICpossibly homozygous112806336
4107137373107137374TC20GENICpossibly homozygous112806338