chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X127580393127580394TC15INTERGENICheterozygous45221242
X127580452127580453CT9INTERGENICheterozygous45221243
X127594565127594566AT19INTERGENICheterozygous45221269
X127661026127661027TA13GENICheterozygous45221378
X127672452127672453AC14GENICheterozygous45221400
X127676566127676567AT9GENICheterozygous45221409
X127686355127686356AG5GENICheterozygous45221445
X127711350127711351TC9GENICheterozygous45221483
X127712641127712642GA6GENICheterozygous45221484
X127730057127730058GA10GENICheterozygous45221499
X127734410127734411TA15GENICheterozygous45221502
X127767814127767815TA12GENICheterozygous45221546
X127768657127768658GT12GENICheterozygous45221547
X127782821127782822GA9GENICheterozygous45221578
X127785742127785743CT37GENICheterozygous45221582
X127789254127789255CCT8GENICheterozygous45221593
X127798965127798966TC15GENICheterozygous45221606
X127807778127807779AC7GENICheterozygous45221668
X127807859127807860CT5GENICheterozygous45221669
X127813222127813223T-19GENICheterozygous45221674
X127813869127813870TC27GENICheterozygous45221675
X127817705127817706G-12GENICheterozygous45221680