chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141058339141058340CCAG46GENIChomozygous55753822
5141058762141058763GGA10GENICheterozygous55753823
5141058762141058763GGAA10GENICheterozygous56457912
5141058812141058813GA24GENIChomozygous55753825
5141059103141059104CT30GENIChomozygous56188106
5141059467141059468GA26GENIChomozygous55753826
5141060465141060466GGAAA18GENIChomozygous55907576
5141062649141062650TTGG37GENIChomozygous55753827
5141063526141063527AT24GENIChomozygous55753828
5141063576141063577CT30GENIChomozygous56188107
5141063618141063620AA--14GENICpossibly homozygous55753829
5141063619141063620A-14GENICheterozygous56457913
5141064520141064521TC34GENIChomozygous56065255
5141064784141064790TGGTGG------6GENIChomozygous56457914
5141067427141067428AT29GENIChomozygous56188108