chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8129467972129467973GA4GENIChomozygous52889531
8129471464129471465GA26GENIChomozygous52889533
8129471515129471516GA28GENIChomozygous52889534
8129471537129471538GA23GENIChomozygous52889535
8129471563129471564TTC23GENIChomozygous52889536
8129471627129471628TC29GENIChomozygous52889537
8129471701129471702GA25GENIChomozygous52889538
8129472470129472471TTACAC1GENIChomozygous52889540
8129473070129473071TTTGTGTGTGTGTG10GENICheterozygous53608097
8129473071129473073TG--10GENICheterozygous53415616
8129475645129475646TTGGG1GENIChomozygous53369678
8129475646129475647CG1GENIChomozygous53369679
8129476893129476894AT22GENIChomozygous52889541
8129479875129479876AAAC2GENIChomozygous52889542
8129480721129480722CG19GENIChomozygous52889544
8129480734129480735CG19GENIChomozygous52889545
8129480745129480746TC24GENIChomozygous52889546
8129480758129480759TG24GENIChomozygous52889547
8129480786129480787G-23GENIChomozygous52889548
8129480788129480789GA25GENIChomozygous53369680
8129480793129480794AC24GENIChomozygous52889549
8129480799129480800A-22GENIChomozygous52889550
8129481514129481515CT28GENIChomozygous52889551
8129482363129482364CT26GENIChomozygous52889552
8129486724129486725GA27GENIChomozygous52889553
8129487861129487862CCA27GENIChomozygous52889554
8129494676129494677AG29GENIChomozygous52889555
8129494881129494882CT24GENIChomozygous52889556
8129495168129495169TTC2GENIChomozygous52889558
8129495930129495931GA32GENIChomozygous52889559
8129472195129472196AC33GENIChomozygous53725878