chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X127661026127661027TA7GENICheterozygous45221378
X127672452127672453AC7GENICheterozygous45221400
X127676566127676567AT6GENICheterozygous45221409
X127711350127711351TC12GENICheterozygous45221483
X127712641127712642GA9GENICheterozygous45221484
X127730057127730058GA12GENICheterozygous45221499
X127734410127734411TA20GENICheterozygous45221502
X127767814127767815TA17GENICheterozygous45221546
X127768657127768658GT16GENICheterozygous45221547
X127785742127785743CT14GENICheterozygous45221582
X127789254127789255CCT12GENICheterozygous45221593
X127798965127798966TC26GENICheterozygous45221606
X127807778127807779AC10GENICheterozygous45221668
X127807859127807860CT10GENICheterozygous45221669
X127813222127813223T-11GENICheterozygous45221674
X127813869127813870TC11GENICheterozygous45221675
X127817705127817706G-9GENICheterozygous45221680
X127873493127873494GA7GENICheterozygous45221766
X127881639127881640CT7GENICheterozygous45221784
X127883962127883963AG16GENICheterozygous45221788
X127885179127885180T-39GENICheterozygous45268162
X127892479127892480CT10GENICheterozygous45221813
X127892498127892499GC7GENICheterozygous45221814
X127896633127896634AG5GENICheterozygous45221826
X127898606127898607TC16GENICheterozygous45221827
X127902764127902765GC20GENICheterozygous45221829
X127903489127903490GA6GENICheterozygous45221830
X127907668127907669AG8GENICheterozygous45221834
X127907764127907767CTG---8GENICheterozygous46000423
X127907771127907772T-8GENICheterozygous45221838
X127907776127907777T-8GENICheterozygous45221839