chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115511069115511070CG12GENICheterozygous927563515
8115513030115513031CT8GENICheterozygous927563516
8115514186115514187CT41GENICheterozygous927563517
8115516330115516331CCG83GENICheterozygous927595787
8115518076115518077AG15GENICheterozygous927563518
8115519250115519251GA13GENICheterozygous927563519
8115527949115527950AC12GENICheterozygous927563520
8115527950115527951GA12GENICheterozygous927563521
8115541589115541590AAG18GENICheterozygous927595788
8115546722115546723AG16GENICheterozygous927563522
8115556364115556365CT12GENICheterozygous927563523
8115557483115557484AG8GENICheterozygous927563524
8115579013115579014TTGG20GENICheterozygous927595789
8115592854115592855AG8GENICheterozygous927563525
8115616477115616478AG22GENICheterozygous927563526
8115630609115630610CT24GENICheterozygous927563527
8115639625115639626TA16GENICheterozygous927563528