chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141058339141058340CCAG38GENIChomozygous55753822
5141058762141058763GGA14GENICpossibly homozygous55753823
5141058775141058779AAAG----17GENIChomozygous56065254
5141058778141058779GGA19GENICpossibly homozygous55753824
5141058779141058780A-19GENICheterozygous55907572
5141062649141062650TTGG28GENIChomozygous55753827
5141064520141064521TC24GENIChomozygous56065255
5141065827141065828CT24GENIChomozygous56065256
5141066478141066479AT23GENIChomozygous56065257