chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155781286257812863TC8GENIChomozygous112521488
155781308757813088TC20GENIChomozygous112521490
155781415057814151AG4GENIChomozygous112521492
155781476957814770TC8GENIChomozygous113054480
155781481157814812CA22GENIChomozygous125778796
155781552557815526GA28GENIChomozygous112521500
155781583457815835TC21GENIChomozygous112521502
155781659257816593GT6GENIChomozygous112521504
155781951857819519AG17GENIChomozygous112521514
155782000657820007CT39GENIChomozygous112521516
155782043057820431GA3GENICheterozygous125834243
155782067757820678GC9GENIChomozygous112521518
155782552657825527CG23GENIChomozygous125778797
155782808257828083AC26GENIChomozygous112521520
155782835857828359GC20GENIChomozygous125778798
155782837857828379GA16GENIChomozygous125778799
155782841857828419TC19GENIChomozygous112521523
155782904057829041TC23GENIChomozygous112521525
155782914957829150TC15GENIChomozygous112521527
155782964857829649AG16GENIChomozygous112521529
155783053857830539GA8GENIChomozygous112521531
155783122357831224AT17GENICpossibly homozygous112521533
155783130657831307GA12GENIChomozygous112521535
155783139257831393GT18GENIChomozygous112521537
155783154357831544CA3GENICheterozygous112809332
155783160757831608TC9GENIChomozygous118920407
155783163257831633TC7GENIChomozygous112919466
155783202457832025GT6GENIChomozygous112521539
155783202557832026CT4GENIChomozygous112521541