chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117255591117255592GA62GENIChomozygous779933982
4117257889117257890CA63GENIChomozygous779933983
4117259437117259438GT22GENICpossibly homozygous779933984
4117264298117264299GA47GENIChomozygous779933985
4117264644117264645CG39GENIChomozygous779933986
4117264803117264804CA31GENIChomozygous779933987
4117266654117266655AG36GENIChomozygous779933988
4117266678117266679GA34GENICpossibly homozygous779933989
4117268193117268194TC51GENIChomozygous779933990
4117269087117269088TC44GENIChomozygous779933991
4117269758117269759CA46GENIChomozygous779933992
4117271188117271189AG57GENICpossibly homozygous779933993
4117271308117271309TA66GENIChomozygous779933994
4117271434117271435TC45GENIChomozygous779933995
4117272285117272286AG42GENIChomozygous779933996
4117274282117274283TG49GENIChomozygous779933997
4117275127117275128AC44GENIChomozygous779933998
4117276347117276348CA64GENIChomozygous779933999
4117277802117277803TA26GENIChomozygous779934000
4117278270117278271GA57GENIChomozygous779934001
4117278981117278982AG55GENIChomozygous779934002
4117279197117279198TC62GENIChomozygous779934003
4117279408117279409TC72GENIChomozygous779934004
4117279581117279582GA57GENIChomozygous779934005
4117279704117279705TC73GENICpossibly homozygous779934006
4117279791117279792AG45GENIChomozygous779934007
4117280030117280031AG43GENIChomozygous779934008
4117280037117280038AG45GENICpossibly homozygous779934009
4117280142117280143GA36GENIChomozygous779934010
4117280653117280654CG82GENIChomozygous779934011
4117281056117281057GA53GENIChomozygous779934012
4117281183117281184GT36GENICpossibly homozygous779934013
4117281563117281564CT58GENIChomozygous779934014
4117281635117281636GT61GENIChomozygous779934015
4117282050117282051TG47GENIChomozygous779934016
4117282268117282269AG43GENIChomozygous779934017
4117282481117282482AC65GENIChomozygous779934018
4117282635117282636TC48GENIChomozygous779934019
4117283800117283801CT63GENIChomozygous779934020
4117284157117284158TC57GENIChomozygous779934021