chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
66422495464224955AT6GENIChomozygous114834520
66422777864227779AG17GENIChomozygous114834522
66422883364228834TC34GENIChomozygous114834524
66423526464235265TA27GENIChomozygous114834526
66423536164235362CT20GENIChomozygous114834528
66423738964237390CT21GENIChomozygous114834530
66423764364237644CT17GENIChomozygous114834532
66423811264238113AG16GENIChomozygous114834534
66423847364238474TA19GENIChomozygous114834538
66423881764238818CT32GENIChomozygous114834540
66423905264239053GT40GENIChomozygous114834542
66423934064239341GC35GENIChomozygous114834544
66423938064239381GT37GENIChomozygous114834546
66424064564240646TC17GENIChomozygous114834548
66424215164242152TC38GENIChomozygous114834550
66425845464258455AG36GENIChomozygous114834580
66425897964258980AG32GENIChomozygous114834582
66425949464259495CG27GENIChomozygous115398582
66426589264265893CT31GENICpossibly homozygous114834584
66426682464266825GA23GENIChomozygous115398584
66427190564271906TC26GENIChomozygous114834588
66427552564275526TC38GENIChomozygous114834592
66427712964277130AG27GENIChomozygous114834598
66428146764281468CT47GENIChomozygous114834602
66428270664282707TC30GENIChomozygous114834604
66428364664283647CA38GENIChomozygous114834606
66428496964284970CT41GENIChomozygous115398586
66428743164287432TA21GENIChomozygous115398588