chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106906980669069807C-14GENICheterozygous51484285
106907010569070106CCTGTG10GENICheterozygous51484287
106907010769070108CG11GENICheterozygous51484288
106907012169070122CG11GENICheterozygous51484289
106907133669071337GA14GENICheterozygous51484291
106907150869071509TG11GENICheterozygous51484292
106907163569071636TA19GENICheterozygous51484293
106907194669071947GC24GENICheterozygous51484294
106907226869072269TTTG17GENICheterozygous51484295
106907259769072598AG19GENICheterozygous51484296
106907302169073022AG10GENICheterozygous51484297
106907364469073645TG11GENICheterozygous51484301
106907398569073986AT17GENICheterozygous51484302
106907403069074031TG15GENICheterozygous51484303
106907405069074051AG9GENICheterozygous51484304
106907409069074091TC9GENICheterozygous51484305
106907414369074144TG12GENICheterozygous51484306
106907433869074339GA15GENICheterozygous51484307