chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117255591117255592GA25GENIChomozygous984959030
4117257889117257890CA10GENIChomozygous984959031
4117264298117264299GA7GENIChomozygous984959032
4117264605117264606AT7GENIChomozygous984959033
4117266654117266655AG13GENIChomozygous984959034
4117266678117266679GA10GENIChomozygous984959035
4117268193117268194TC4GENIChomozygous984959036
4117271188117271189AG18GENIChomozygous984959037
4117271434117271435TC16GENIChomozygous984959038
4117272285117272286AG14GENIChomozygous984959039
4117274282117274283TG26GENIChomozygous984959040
4117275127117275128AC19GENIChomozygous984959041
4117276347117276348CA18GENIChomozygous984959042
4117278270117278271GA20GENIChomozygous984959043
4117279197117279198TC12GENIChomozygous984959044
4117279408117279409TC25GENIChomozygous984959045
4117279581117279582GA26GENIChomozygous984959046
4117279791117279792AG23GENIChomozygous984959047
4117280030117280031AG28GENIChomozygous984959048
4117280037117280038AG26GENIChomozygous984959049
4117280142117280143GA11GENIChomozygous984959050
4117280653117280654CG16GENIChomozygous984959051
4117281056117281057GA14GENIChomozygous984959052
4117281563117281564CT23GENIChomozygous984959053
4117281635117281636GT12GENIChomozygous984959054
4117282050117282051TG23GENIChomozygous984959055
4117282268117282269AG24GENIChomozygous984959056
4117282481117282482AC25GENIChomozygous984959057
4117282635117282636TC22GENIChomozygous984959058
4117283800117283801CT19GENIChomozygous984959059
4117284157117284158TC19GENIChomozygous984959060