chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141058339141058340CCAG44GENIChomozygous55753822
5141058762141058763GGA7GENIChomozygous55753823
5141058778141058779GGA14GENIChomozygous55753824
5141058812141058813GA17GENIChomozygous55753825
5141059467141059468GA20GENIChomozygous55753826
5141062649141062650TTGG43GENIChomozygous55753827
5141063526141063527AT44GENIChomozygous55753828
5141063618141063620AA--22GENICpossibly homozygous55753829
5141063619141063620A-22GENICheterozygous56457913
5141063765141063766AG26GENIChomozygous55753830
5141066515141066516GT25GENIChomozygous55753831
5141068528141068529TTAATA3GENIChomozygous55753832
5141069921141069922GT36GENIChomozygous55753833
5141070769141070770CT12GENIChomozygous55753834