chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118873091118873092AG58GENIChomozygous138433515
8118873606118873607TC59GENIChomozygous138433517
8118873618118873619CT57GENIChomozygous142104936
8118874133118874134TC61GENIChomozygous138433519
8118874438118874439G43GENIChomozygous138268841
8118874441118874443GG43GENIChomozygous138268842
8118874504118874505TG42GENICpossibly homozygous142104937
8118874533118874534CT50GENICheterozygous403959242
8118874539118874540CT52GENICheterozygous403959243
8118875546118875547AC56GENIChomozygous138433521
8118876080118876081TC49GENIChomozygous138433523
8118876280118876281AG44GENIChomozygous138433524
8118877517118877518TA44GENIChomozygous138433525
8118877667118877668TC46GENIChomozygous138433526
8118877676118877677AC47GENIChomozygous138433527
8118879387118879388AG48GENIChomozygous138433528
8118880037118880038TC47GENIChomozygous138433529
8118880514118880515TC40GENIChomozygous138433532
8118880927118880928GA47GENIChomozygous138433533
8118880943118880943GTG43GENIChomozygous138268844
8118881164118881166CA50GENIChomozygous142031663
8118881289118881290TA61GENICpossibly homozygous138433534
8118881401118881402GA44GENIChomozygous142104938
8118881415118881416GA38GENIChomozygous142104939
8118881765118881766GA56GENIChomozygous145146663