chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X127661026127661027TA22GENICheterozygous45221378
X127672452127672453AC11GENICheterozygous45221400
X127676566127676567AT9GENICheterozygous45221409
X127686355127686356AG10GENICheterozygous45221445
X127711350127711351TC11GENICheterozygous45221483
X127712641127712642GA7GENICheterozygous45221484
X127734410127734411TA14GENICheterozygous45221502
X127767814127767815TA8GENICheterozygous45221546
X127768657127768658GT8GENICheterozygous45221547
X127782821127782822GA9GENICheterozygous45221578
X127785742127785743CT18GENICheterozygous45221582
X127789254127789255CCT8GENICheterozygous45221593
X127789561127789562CT24GENICheterozygous45463071
X127798965127798966TC21GENICheterozygous45221606
X127807778127807779AC12GENICheterozygous45221668
X127807859127807860CT7GENICheterozygous45221669
X127813222127813223T-10GENICheterozygous45221674
X127813869127813870TC14GENICheterozygous45221675
X127839589127839590GA9GENICheterozygous45221720
X127873493127873494GA11GENICheterozygous45221766
X127883962127883963AG11GENICheterozygous45221788
X127885179127885180T-24GENICheterozygous45268162
X127892479127892480CT6GENICheterozygous45221813
X127896633127896634AG9GENICheterozygous45221826
X127898606127898607TC29GENICheterozygous45221827
X127902764127902765GC36GENICheterozygous45221829
X127903489127903490GA13GENICheterozygous45221830
X127907668127907669AG7GENICheterozygous45221834
X127907764127907767CTG---7GENICheterozygous46000423
X127907771127907772T-7GENICheterozygous45221838
X127907776127907777T-7GENICheterozygous45221839