chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
526078392607840AG40GENIChomozygous113626622
526092502609251TC57GENIChomozygous113626624
526095802609581GA49GENIChomozygous114321359
526098122609813TC54GENIChomozygous113626625
526100402610041TC66GENIChomozygous114321361
526104002610401GA48GENIChomozygous114321363
526112252611226TG49GENIChomozygous114321365
526118432611844GT48GENIChomozygous113626627
526119202611921CT52GENIChomozygous114321367
526124322612433CT46GENIChomozygous114321369
526125782612579TC77GENIChomozygous114321371
526133972613398CG65GENIChomozygous114321373
526136612613662AG55GENIChomozygous113626628
526142092614211AA23GENIChomozygous128144191
526154422615443TC29GENICpossibly homozygous114321379
526157772615778TG44GENIChomozygous114321381
526158822615883GA49GENICpossibly homozygous114321383
526159082615909CT54GENICpossibly homozygous114321385
526160972616098AG53GENICpossibly homozygous114321387
526164032616404CG48GENICpossibly homozygous114321389
526177582617759CA63GENIChomozygous114321391
526183152618316GA56GENIChomozygous114321393
526188662618867TG34GENIChomozygous113626638
526188692618870TA33GENIChomozygous113626639
526107432610744CG13GENIChomozygous122446519
526197372619738CT49GENIChomozygous114321395
526203802620381AC69GENICpossibly homozygous114321397
526207452620746AG56GENIChomozygous114321399
526210972621098GC42GENIChomozygous114321401
526211702621171AT47GENIChomozygous113626643
526211722621173AT46GENIChomozygous113626644
526225832622584AG68GENIChomozygous114321403
526228442622845GA58GENIChomozygous114321405
526236382623639TG74GENIChomozygous113626648
526243762624377TG52GENIChomozygous113626649
526244352624436AG56GENIChomozygous113626650
526249822624983CT73GENIChomozygous114321407
526259322625933CA78GENIChomozygous114321409
526287962628797AT70GENIChomozygous113626652
526294572629458CT61GENIChomozygous113626653
526296592629660CT61GENIChomozygous113626654
526313302631331AC66GENIChomozygous113626655
526189012618921TGTTTGTGTGTGTGTGGTGT15GENIChomozygous131852632