chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2240626970240626971CG23GENIChomozygous110334626
2240629018240629019AC25GENIChomozygous110334628
2240629350240629351TC61GENIChomozygous110334630
2240629475240629476TC56GENIChomozygous110334632
2240629823240629824AG70GENIChomozygous110334634
2240630554240630555CA68GENIChomozygous110334636
2240631606240631607TC56GENIChomozygous110334638
2240632450240632451TA90GENIChomozygous110334640
2240633212240633213AT81GENIChomozygous110334642
2240633781240633782GA61GENIChomozygous110334644
2240634792240634793TG66GENIChomozygous110334646
2240636244240636245AG87GENIChomozygous110334648
2240636537240636538TG71GENIChomozygous110334650
2240636763240636764GA58GENIChomozygous110334652
2240638992240638993GA64GENIChomozygous110334654
2240639143240639144GA75GENIChomozygous110334656
2240639524240639525TC85GENIChomozygous110334658
2240642744240642745CT95GENIChomozygous110334660
2240646082240646083GA78GENIChomozygous110334668
2240642780240642781GT89GENIChomozygous110334662
2240629028240629029AG25GENIChomozygous110632336
2240629035240629036CT19GENIChomozygous110632338
2240629061240629062CT24GENICheterozygous110632340
2240631800240631801TG80GENICpossibly homozygous110632342
2240643623240643624AG65GENICpossibly homozygous110334664
2240645839240645840GA76GENIChomozygous110334666
2240646549240646550GA78GENIChomozygous110334670
2240647279240647280AG82GENIChomozygous110334672
2240647404240647405CT80GENIChomozygous110334674
2240647967240647968CT83GENIChomozygous110334676
2240650194240650195AG68GENIChomozygous110334678
2240651105240651106CT48GENIChomozygous110334680
2240651673240651674AG44GENIChomozygous110334682
2240652833240652834AC43GENICpossibly homozygous110334684