chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7138917947138917948GA43GENICheterozygous54143903
7138918022138918023CT41GENICheterozygous54143905
7138918135138918136CA39GENICheterozygous54143907
7138918623138918624CT38GENICpossibly homozygous54143908
7138919112138919113GA83GENICheterozygous54143910
7138919116138919117CT84GENICheterozygous54143912
7138919134138919135AG86GENICheterozygous54143914
7138919218138919219AG72GENICheterozygous54143916
7138919846138919847AG30GENIChomozygous54143917
7138920299138920300CCTT12GENIChomozygous54143921
7138920317138920318CT21GENICheterozygous54143923
7138920928138920929AC29GENIChomozygous54143925
7138922492138922493T-4GENICheterozygous54526568
7138922803138922804CT22GENIChomozygous54143930
7138923305138923306T-14GENIChomozygous54143932
7138924080138924081GA22GENIChomozygous54143934
7138924358138924359AG21GENIChomozygous54143936
7138936175138936176AG42GENICpossibly homozygous54143937