chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117255591117255592GA19GENIChomozygous966603652
4117257889117257890CA23GENIChomozygous966603653
4117264298117264299GA25GENIChomozygous966603654
4117264605117264606AT15GENIChomozygous966603655
4117264644117264645CG16GENIChomozygous966603656
4117265590117265591CA25GENIChomozygous966603657
4117266654117266655AG16GENIChomozygous966603658
4117266678117266679GA15GENIChomozygous966603659
4117271308117271309TA16GENIChomozygous966603660
4117272285117272286AG11GENICpossibly homozygous966603661
4117274282117274283TG17GENIChomozygous966603662
4117275127117275128AC17GENICpossibly homozygous966603663
4117276347117276348CA22GENIChomozygous966603664
4117277802117277803TA11GENIChomozygous966603665
4117278270117278271GA23GENIChomozygous966603666
4117278981117278982AG11GENIChomozygous966603667
4117279197117279198TC20GENICpossibly homozygous966603668
4117279408117279409TC18GENIChomozygous966603669
4117279581117279582GA36GENICpossibly homozygous966603670
4117279704117279705TC35GENICpossibly homozygous966603671
4117279791117279792AG40GENIChomozygous966603672
4117280030117280031AG29GENIChomozygous966603673
4117280037117280038AG25GENIChomozygous966603674
4117280142117280143GA39GENIChomozygous966603675
4117280290117280291TC8GENIChomozygous966603676
4117280292117280293TG7GENIChomozygous966603677
4117280299117280300AT6GENIChomozygous966603678
4117280653117280654CG15GENIChomozygous966603679
4117281056117281057GA25GENIChomozygous966603680
4117281183117281184GT22GENIChomozygous966603681
4117281563117281564CT19GENICpossibly homozygous966603682
4117281635117281636GT23GENICpossibly homozygous966603683
4117282050117282051TG20GENIChomozygous966603684
4117282268117282269AG31GENICpossibly homozygous966603685
4117282481117282482AC31GENIChomozygous966603686
4117282635117282636TC29GENICpossibly homozygous966603687
4117283800117283801CT33GENIChomozygous966603688
4117284157117284158TC14GENICpossibly homozygous966603689