chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
473099187309919TC10GENIChomozygous60126627
473110607311061CT11GENIChomozygous60126629
473122237312224CT23GENICheterozygous60126631
473122927312293TTTC18GENIChomozygous60126633
473126047312605TC14GENIChomozygous60126635
473128917312892TC14GENIChomozygous60126638
473129777312978C-13GENIChomozygous60126640
473137127313713AG14GENIChomozygous60126642
473139367313937CT8GENIChomozygous60126644
473140977314098AT15GENIChomozygous60126646
473146427314643TC18GENIChomozygous60126649
473147937314794CT19GENIChomozygous60126651
473152747315275AG14GENIChomozygous60126653
473156517315652TC12GENIChomozygous60126655
473158117315812TA15GENIChomozygous60126657
473160527316053TC17GENIChomozygous60126660
473162107316211GA12GENIChomozygous60126662
473164377316438AG8GENIChomozygous60126664
473167187316719GA7GENIChomozygous60126666
473173197317320AG9GENIChomozygous60126668
473175267317527AG12GENIChomozygous60126670
473183297318330GC9GENIChomozygous60126672
473187487318749TC11GENIChomozygous60126675
473188027318803AT11GENIChomozygous60126677
473191287319129CT17GENIChomozygous60126679
473193727319373GT25GENIChomozygous60126682
473194957319496CG12GENIChomozygous60126684
473194977319498CT13GENIChomozygous60126686
473198887319889TC10GENIChomozygous60126688
473199017319902TG12GENIChomozygous60126690
473204217320422TA9GENIChomozygous60126693
473205067320507GC11GENIChomozygous60126695
473205237320524AG11GENIChomozygous60126697
473207977320798G-9GENIChomozygous60126699
473211677321168TC21GENIChomozygous60126701
473212037321204GA16GENIChomozygous60126703
473217187321719AAAAAAAAAG12GENIChomozygous60126705
473218587321859A-12GENIChomozygous60126708
473227607322761TC12GENIChomozygous60126710
473228427322843CT15GENIChomozygous60126712