chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4100760829100760830TG38GENIChomozygous113284634
4100763329100763330CT24GENICpossibly homozygous113537959
4100764153100764154AT7GENIChomozygous113284635
4100764723100764724TC21GENIChomozygous113284636
4100766148100766149AG27GENICpossibly homozygous113284637
4100766188100766189GC21GENIChomozygous113284638
4100766330100766331AC23GENICpossibly homozygous113537961
4100766335100766336AC21GENICpossibly homozygous113537963
4100766482100766483AT36GENIChomozygous113284639
4100769942100769943CA20GENIChomozygous113537967
4100771125100771126GA25GENIChomozygous113284642
4100771206100771207AG28GENIChomozygous113284643
4100774677100774678AG39GENICheterozygous113284646
4100774695100774696GA33GENICheterozygous113537971
4100774701100774702GA32GENICheterozygous113537973
4100775697100775698CG42GENIChomozygous112798864
4100776161100776162CT30GENICpossibly homozygous113537975
4100778471100778472TC42GENICpossibly homozygous113284649
4100780020100780021AC41GENIChomozygous113537979
4100780799100780800TC27GENIChomozygous113284650
4100782302100782303TA10GENIChomozygous113284651