chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6127285407127285408CG17GENICpossibly homozygous118734727
6127288672127288673AG28GENIChomozygous114982985
6127290199127290200TC18GENIChomozygous114982986
6127292017127292018AG28GENIChomozygous114982990
6127292721127292722AG24GENIChomozygous114982991
6127295874127295875GA21GENIChomozygous118734729
6127296407127296408AC11GENIChomozygous114983003
6127296998127296999TC27GENIChomozygous118734730
6127297020127297021AG30GENIChomozygous114983006
6127297510127297511AT23GENIChomozygous114983009
6127297829127297830GT27GENIChomozygous114983011
6127297831127297832AG26GENIChomozygous114983012
6127298424127298425GA20GENIChomozygous114983015
6127298429127298430AG21GENIChomozygous114983016
6127298563127298564TC26GENIChomozygous118734731
6127298599127298600AG21GENIChomozygous114983018
6127298622127298623TC12GENIChomozygous114983020
6127298795127298796TC23GENIChomozygous114983021
6127298876127298877AG17GENIChomozygous114983022
6127299598127299599AT24GENIChomozygous114983023
6127299783127299784GA31GENIChomozygous118734732
6127300174127300175AC26GENIChomozygous114983027
6127300328127300329AC28GENIChomozygous114983028
6127300538127300539TC30GENIChomozygous114983029
6127300563127300564CT28GENIChomozygous118734733
6127300997127300998AG21GENIChomozygous114983031
6127301031127301032CG23GENIChomozygous114983032