chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104343578243435782C9GENIChomozygous129968842
104343588643435886C20GENIChomozygous128812868
104343590043435900G20GENIChomozygous128812869
104343600543436005C7GENIChomozygous128812870
104343602743436027G5GENIChomozygous128812871
104344717843447179TC50GENIChomozygous116766314
104344797443447975G31GENIChomozygous130776709
104344808243448083GC19GENIChomozygous123350394
104344881343448814GA38GENIChomozygous116766318
104344909843449099AC51GENIChomozygous123350397
104345054943450550GA45GENIChomozygous116766322
104345545643455457C49GENIChomozygous128812872
104344810743448108AG24GENIChomozygous117128316
104344887243448873AT36GENIChomozygous116875757
104345846843458469GA43GENIChomozygous116875759
104345884143458842TA47GENIChomozygous116875761
104344906543449065C43GENICpossibly homozygous131092285
104345757843457586AGTCAGTC40GENIChomozygous131092286
104344967743449678GA47GENIChomozygous116578837
104346062243460622A47GENIChomozygous128812875
104346439943464399A60GENIChomozygous128812876
104347019143470228TACCTACTTTCTTAATTGATTGTGAAACACTATTGGG33GENIChomozygous128812877
104347595443475954C53GENIChomozygous131092287
104347913743479138TG38GENIChomozygous116875763
104348095343480953G36GENIChomozygous128812878
104349312943493129C48GENIChomozygous128812879
104349326343493264T50GENIChomozygous128812880
104349329743493299CC47GENIChomozygous128812881
104349333043493331CT40GENIChomozygous116578843
104349441143494412AG14GENIChomozygous116578845
104349442643494427TG15GENIChomozygous116578847
104349506943495070CT46GENIChomozygous116875765
104349863043498630A11GENIChomozygous131092288
104350004543500046TC37GENIChomozygous116766374
104346233043462331TG8GENIChomozygous128868359
104346326543463266T2GENIChomozygous132145217
104346386143463862TC2GENICheterozygous132490543
104346386543463866TC2GENICheterozygous132490544