chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101419619114196193CA--12GENICpossibly homozygous697647775
101419645714196458GC30GENIChomozygous541169827
101419645814196459TTG30GENIChomozygous697647776
101419839514198396TA30GENICheterozygous541169828
101421459614214597GGT9GENICheterozygous697647777
101421860014218601TC36GENIChomozygous538613792
101423007014230071G-34GENICheterozygous697647779
101424054514240546TC24GENIChomozygous538613793
101424568514245686C-18GENICheterozygous697647781
101424836414248369TGGTT-----18GENICheterozygous697647782
101425256014252564GTGT----15GENICheterozygous697647783
101425364514253646TTTAA1GENIChomozygous697647784
101426633514266336AT18GENICheterozygous541169829
101426634514266346TG16GENICheterozygous538613794
101426636514266366G-13GENIChomozygous697647787