chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101077510110775102GA13GENICheterozygous116493695
101077535110775352TC14GENICheterozygous116493697
101077570110775701TTTTG18GENICheterozygous131087101
101077615410776155AG20GENICheterozygous116493699
101077626810776269CT10GENICheterozygous116493701
101077683710776838CT18GENICheterozygous116493703
101077739010777391CT17GENICheterozygous116493705
101077743310777434GA15GENICheterozygous116493707
101077819410778195TG19GENICheterozygous116493709
101077819610778197GT19GENICheterozygous116493711
101077840410778484ACACACATACACACACATATACACACACATACATACACACATAAGCACATACATACACACACATACACACACACATACAC13GENICheterozygous131087102
101077944810779449AG11GENICheterozygous116493713
101077970610779707CT8GENICheterozygous117102508
101077971910779720CT9GENICheterozygous117140125
101077980410779805GA15GENICheterozygous116493715
101078029410780295CT21GENICheterozygous118026519
101078038210780383GA23GENICheterozygous116493717
101078041210780413TA20GENICheterozygous116493719
101078041310780414CA19GENICheterozygous116493721
101078161210781613TC27GENICheterozygous116993885
101078273610782737TC22GENICheterozygous116493723
101078280410782805GA25GENICheterozygous116493725
101078407410784075AG25GENICheterozygous116493729
101078417610784177GA27GENICheterozygous116993886