chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160306835160306836TA42GENIChomozygous114074068
5160306998160306999AG33GENICpossibly homozygous114074069
5160307587160307588CT24GENIChomozygous114074070
5160311173160311174GT20GENIChomozygous114074071
5160312395160312396CT27GENIChomozygous114074072
5160312812160312813CT26GENIChomozygous114074073
5160312941160312942AG16GENIChomozygous114074074
5160313457160313458AG17GENIChomozygous114074075
5160313740160313741TC30GENIChomozygous114074076
5160315544160315545CT21GENIChomozygous114074077
5160315662160315663CT15GENICpossibly homozygous114074078
5160316358160316359AG27GENIChomozygous114074079
5160317118160317119AG26GENIChomozygous114074080
5160321176160321177TA29GENICpossibly homozygous114074081