chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X127580393127580394TC12INTERGENICheterozygous45221242
X127580452127580453CT12INTERGENICheterozygous45221243
X127594565127594566AT9INTERGENICheterozygous45221269
X127661026127661027TA14GENICheterozygous45221378
X127676566127676567AT7GENICheterozygous45221409
X127686355127686356AG6GENICheterozygous45221445
X127711350127711351TC12GENICheterozygous45221483
X127712641127712642GA5GENICheterozygous45221484
X127730057127730058GA7GENICheterozygous45221499
X127734410127734411TA11GENICheterozygous45221502
X127767814127767815TA11GENICheterozygous45221546
X127768657127768658GT11GENICheterozygous45221547
X127782821127782822GA12GENICheterozygous45221578
X127785742127785743CT10GENICheterozygous45221582
X127789254127789255CCT9GENICheterozygous45221593
X127789561127789562CT15GENICheterozygous45463071
X127798965127798966TC19GENICheterozygous45221606
X127807778127807779AC15GENICheterozygous45221668
X127813222127813223T-20GENICheterozygous45221674
X127813869127813870TC9GENICheterozygous45221675