chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4208737365208737366GA11GENIChomozygous57066926
4208739469208739470AG13GENICpossibly homozygous57066927
4208740313208740314TA14GENICpossibly homozygous57066928
4208740848208740849TC20GENICheterozygous57066929
4208741273208741274AG12GENIChomozygous57066932
4208741670208741671CT23GENIChomozygous57066933
4208743356208743358TG--4GENICheterozygous58487748
4208745609208745610CA14GENIChomozygous57066938