chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81330646513306466CT8GENICpossibly homozygous53090868
81330665813306659CT10GENICpossibly homozygous53090869
81330699213306993TC18GENICpossibly homozygous53090870
81330912613309127TC4GENIChomozygous53090877
81330913913309140GA4GENICheterozygous53090878
81331108513311086GA16GENIChomozygous53090880
81331129513311296CT17GENICpossibly homozygous53090881
81331165513311656AG9GENIChomozygous53090882
81331226813312269TG5GENICheterozygous53090883
81331227213312273TC5GENIChomozygous53090884
81331245413312455GA13GENICpossibly homozygous53090886
81331295613312957TC19GENIChomozygous53090887
81331329113313292AACACT4GENIChomozygous53090888
81331347213313473GC16GENICpossibly homozygous53090889
81331372113313722GA17GENICpossibly homozygous53090890
81331412213314123TC19GENICpossibly homozygous53090891
81331439813314399CT12GENICpossibly homozygous53090892
81331511613315117CT15GENICpossibly homozygous53090893
81331537113315372AAGAGAG8GENICheterozygous53614711
81331539213315393TTAGGGG10GENICheterozygous53614712
81331577213315773TA8GENIChomozygous53090895
81331582413315825TA13GENICheterozygous53090896
81331590913315910TC15GENIChomozygous53090897
81331624613316247A-13GENIChomozygous53373243