chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1117574104117574105AG19GENIChomozygous125283491
1117574567117574568TC16GENIChomozygous125366044
1117574919117574920AT5GENIChomozygous125399072
1117574921117574922TA7GENIChomozygous125399074
1117575489117575490GA18GENIChomozygous125366045
1117575762117575763CT12GENIChomozygous125283493
1117576344117576345TC18GENIChomozygous125283494
1117576369117576370AG20GENIChomozygous125283495
1117576627117576628TA10GENIChomozygous125366046
1117576802117576803AG14GENIChomozygous125283496
1117576906117576907TG13GENIChomozygous125366047
1117577149117577150AG16GENIChomozygous125283497
1117577562117577563CT15GENIChomozygous125366048
1117577678117577679CT12GENIChomozygous125366049
1117578849117578850AC15GENIChomozygous125283503
1117579182117579183AG16GENIChomozygous125366050
1117579839117579840AC11GENIChomozygous125283506
1117579879117579880GT10GENIChomozygous125366051
1117581111117581112AC20GENIChomozygous125366052
1117581410117581411TG24GENIChomozygous125283510
1117581649117581650GC6GENICheterozygous125283511
1117581766117581767TA11GENIChomozygous125283512
1117582039117582040CT13GENIChomozygous125366053
1117582435117582436AG11GENIChomozygous125366054
1117582457117582458CT6GENIChomozygous125366055
1117583339117583340CA6GENIChomozygous125366056
1117585358117585359AC10GENIChomozygous125283515
1117585674117585675AG22GENIChomozygous125283517
1117586475117586476AG13GENIChomozygous125283521
1117586819117586820AC10GENIChomozygous125399076
1117586867117586868GT19GENIChomozygous125283522
1117587176117587177TC5GENIChomozygous125366057