chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X127580393127580394TC9INTERGENICheterozygous45221242
X127580452127580453CT10INTERGENICheterozygous45221243
X127594565127594566AT7INTERGENICheterozygous45221269
X127661026127661027TA10GENICheterozygous45221378
X127672452127672453AC14GENICheterozygous45221400
X127676566127676567AT11GENICheterozygous45221409
X127711350127711351TC12GENICheterozygous45221483
X127712641127712642GA9GENICheterozygous45221484
X127730057127730058GA9GENICheterozygous45221499
X127734410127734411TA5GENICheterozygous45221502
X127767814127767815TA16GENICheterozygous45221546
X127768657127768658GT12GENICheterozygous45221547
X127782821127782822GA8GENICheterozygous45221578
X127785742127785743CT14GENICheterozygous45221582
X127798965127798966TC22GENICheterozygous45221606
X127807778127807779AC14GENICheterozygous45221668
X127807859127807860CT15GENICheterozygous45221669
X127813222127813223T-9GENICheterozygous45221674
X127813869127813870TC24GENICheterozygous45221675