chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69342369993423700TC42GENICpossibly homozygous115139376
69342389893423899GA12GENICheterozygous114903420
69342471193424712AG27GENIChomozygous115139378
69342516193425162AG20GENIChomozygous115139379
69342522693425227CT55GENICheterozygous115139380
69342528793425288GC38GENICpossibly homozygous115139381
69342621593426216TC45GENICheterozygous114903428
69343041293430413AG25GENIChomozygous115139382
69343203793432038GA44GENIChomozygous114903430
69343323593433236AT39GENIChomozygous115139384
69343386593433866TA51GENICpossibly homozygous114903434
69343643193436432TC12GENICheterozygous115139385
69343643293436433GA12GENICheterozygous115139386
69343643993436440TA15GENICheterozygous115139387
69343645493436455GA16GENICheterozygous114903438
69343650293436503CT20GENICheterozygous114903440
69343650493436505GA20GENICheterozygous114903442
69343652093436521CT27GENICheterozygous114903444
69343654393436544GT27GENIChomozygous114903446
69343654993436550CT24GENIChomozygous114903448
69343658993436590CG29GENIChomozygous114903450
69343677993436780CT42GENIChomozygous115139388
69343724293437243GT54GENIChomozygous114903454
69343753993437540GA66GENIChomozygous115139389
69344083493440835TC53GENICheterozygous114903460
69344086793440868AG58GENICheterozygous114903462
69344087593440876GT58GENICheterozygous114903464
69344174393441744TC56GENICpossibly homozygous115139390
69344297993442980TC68GENIChomozygous115139391