chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104706689247066893AG15GENIChomozygous955782012
104706738747067388TC32GENIChomozygous955782013
104706760647067607GA18GENIChomozygous955782014
104706850747068508AG16GENIChomozygous955782015
104708237347082374GA23GENIChomozygous955782016
104708308147083082GA32GENIChomozygous955782017
104708367247083673TC18GENIChomozygous955782018
104708432247084323AG15GENIChomozygous955782019
104708446147084462TC19GENIChomozygous955782020
104708510747085108GA41GENIChomozygous955782021
104708587347085874TC50GENIChomozygous955782022
104708642247086423GC29GENIChomozygous955782023
104708650047086501AG27GENIChomozygous955782024
104708655247086553CT26GENIChomozygous955782025
104708665247086653CA21GENIChomozygous955782026
104708734847087349GA32GENIChomozygous955782027
104708819347088194GT25GENIChomozygous955782028
104708996147089962TC12GENIChomozygous955782029
104709009547090096TA8GENIChomozygous955782030
104709123347091234GA29GENIChomozygous955782031
104709128847091289GT30GENIChomozygous955782032
104709132947091330GA32GENIChomozygous955782033
104709153347091534CT31GENIChomozygous955782034
104709296347092964TC22GENIChomozygous955782035
104709340547093406AG15GENIChomozygous955782036
104709355047093551CA20GENIChomozygous955782037
104709355247093553TC20GENIChomozygous955782038
104709370847093709TC23GENIChomozygous955782039
104709401947094020TC14GENIChomozygous955782040
104709432547094326TA29GENIChomozygous955782041
104709540047095401AC26GENIChomozygous955782042
104709700447097005TC35GENIChomozygous955782043
104709953547099536TA24GENICpossibly homozygous955782044
104710175847101759CT17GENIChomozygous955782045
104710472647104727GA37GENIChomozygous955782046
104710532847105329TC41GENIChomozygous955782047
104710603047106031TC26GENIChomozygous955782048
104710799847107999AG25GENIChomozygous955782049
104710810447108105CG28GENIChomozygous955782050
104711059447110595GC19GENIChomozygous955782051