chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6146170707146170708AC5GENIChomozygous54766895
6146172666146172667TC22GENIChomozygous54766896
6146172846146172847CT16GENICpossibly homozygous54766897
6146172924146172925AG19GENICpossibly homozygous54766898
6146173451146173452TC13GENICpossibly homozygous54766899
6146174940146174941TC13GENIChomozygous54766900
6146176840146176841TC19GENICpossibly homozygous54766902
6146180433146180434CT6GENICheterozygous55780190
6146183568146183569CA10GENIChomozygous55780192
6146183686146183687GA10GENICpossibly homozygous55780194
6146186029146186030CT19GENIChomozygous55780196
6146186174146186181TTTTGTT-------2GENIChomozygous55780198
6146186809146186810AG7GENIChomozygous54766912
6146187581146187582TG16GENICpossibly homozygous54766913