chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
23494685134946852GA25GENIChomozygous109690531
23494699834946999AG22GENIChomozygous109690533
23494701834947019AG22GENIChomozygous109690535
23494719334947194GA24GENIChomozygous109690537
23494731634947317GC41GENIChomozygous109690539
23494738534947386TA49GENIChomozygous109690541
23494750534947506AG54GENIChomozygous109690543
23494808834948089AG51GENIChomozygous109690545
23494811934948120TA52GENIChomozygous109690547
23494812934948130AG47GENIChomozygous109690549
23494822234948223TG32GENIChomozygous109690551
23494876934948770GA35GENIChomozygous109690553
23494889734948898CT44GENIChomozygous109690555
23494954634949547GA38GENIChomozygous109690557
23494961834949619GA54GENIChomozygous109690559
23494996434949965AG25GENIChomozygous109690561
23495106834951069TC31GENIChomozygous109690571
23495134834951349CT20GENIChomozygous109690572
23495738934957390CT17GENIChomozygous109690586
23495761134957612TC33GENIChomozygous109690588
23495778434957785CA30GENIChomozygous109690590
23495805834958059TC27GENIChomozygous109690592
23495835434958355TC25GENIChomozygous109690594
23495837934958380CT25GENICpossibly homozygous109690596
23495839034958391AC26GENIChomozygous109690598
23495854634958547AG45GENIChomozygous109690600
23495866834958669TC26GENIChomozygous109690602
23495868734958688TC30GENIChomozygous109690604
23495871234958713AG31GENIChomozygous109690606
23495873534958736TC30GENIChomozygous109690607
23495943334959434TC35GENIChomozygous109690609
23495943934959440AG37GENIChomozygous109690611
23495947434959475GA31GENIChomozygous109690613
23495972134959722GA25GENIChomozygous109690615
23496205634962057GC26GENIChomozygous109690617
23496355234963553AC47GENIChomozygous109690621
23496376834963769TC38GENIChomozygous109690623
23496418134964182TC35GENIChomozygous109690625
23496474934964750TC61GENIChomozygous109690627
23496490634964907CA48GENIChomozygous109690629
23496515634965157GA46GENIChomozygous109690631
23496535134965352TA43GENIChomozygous109690633