chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4183879220183879221T18GENIChomozygous128116525
4183879307183879308T15GENIChomozygous128116526
4183879397183879398T14GENIChomozygous128116527
4183879967183879968AG21GENIChomozygous112982803
4183880040183880041GA14GENIChomozygous112982805
4183880624183880624T10GENIChomozygous128116528
4183881255183881256C17GENIChomozygous128116529
4183881551183881552TG8GENIChomozygous113069421
4183881559183881560T7GENIChomozygous128116530
4183881572183881573GA9GENIChomozygous112982807
4183882880183882881GA12GENIChomozygous112982809
4183883251183883252AG14GENIChomozygous112982813
4183883659183883660TC16GENIChomozygous112982815
4183884576183884577TA16GENIChomozygous112982817
4183886019183886020TC17GENIChomozygous112982819
4183886889183886890GT27GENIChomozygous112982821
4183889240183889245GGGTA11GENIChomozygous128116531
4183889583183889584CA21GENIChomozygous112982823
4183890241183890242T20GENIChomozygous128116532
4183890462183890463CT8GENIChomozygous112982825
4183890863183890864GA19GENIChomozygous112982827
4183892111183892114CTT22GENIChomozygous128116533
4183893522183893523TC22GENIChomozygous112982829
4183894191183894192CA16GENIChomozygous119456259
4183894193183894194CA17GENIChomozygous119467142
4183894195183894196CA17GENIChomozygous119467143
4183894197183894198CA17GENIChomozygous119467144
4183900174183900175AC15GENIChomozygous112982831
4183900225183900226AG17GENIChomozygous112982833
4183901500183901501T12GENICpossibly homozygous128116534
4183901778183901779AG20GENIChomozygous112982835
4183901853183901854AT19GENIChomozygous112982837
4183901958183901959GA16GENIChomozygous112982839
4183901983183901984GT19GENIChomozygous112982841
4183905208183905209TC12GENIChomozygous112982843