chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8129467972129467973GA6GENIChomozygous52889531
8129471464129471465GA13GENICpossibly homozygous52889533
8129471515129471516GA2GENIChomozygous52889534
8129471537129471538GA7GENIChomozygous52889535
8129471563129471564TTC14GENIChomozygous52889536
8129471627129471628TC15GENIChomozygous52889537
8129471701129471702GA20GENICpossibly homozygous52889538
8129475645129475646TTGGG1GENIChomozygous53369678
8129475646129475647CG1GENIChomozygous53369679
8129476893129476894AT18GENIChomozygous52889541
8129480721129480722CG10GENICheterozygous52889544
8129480734129480735CG5GENIChomozygous52889545
8129480745129480746TC4GENIChomozygous52889546
8129480758129480759TG5GENIChomozygous52889547
8129480786129480787G-3GENIChomozygous52889548
8129480788129480789GA3GENIChomozygous53369680
8129480793129480794AC5GENIChomozygous52889549
8129480799129480800A-4GENIChomozygous52889550
8129481514129481515CT15GENICpossibly homozygous52889551
8129482363129482364CT19GENIChomozygous52889552
8129486724129486725GA23GENICpossibly homozygous52889553
8129487861129487862CCA5GENICheterozygous52889554
8129494676129494677AG15GENICpossibly homozygous52889555
8129494881129494882CT29GENIChomozygous52889556
8129494973129494974GA18GENICpossibly homozygous52889557
8129495930129495931GA25GENIChomozygous52889559