chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108897970888979709CA12INTERGENIChomozygous68157653
108897974288979743CG18INTERGENICheterozygous68157657
108898317688983177TG15GENIChomozygous68157660
108898355788983558TG17GENICheterozygous68157683
108898415788984158AG6GENIChomozygous68157694
108898446788984468AG6GENIChomozygous68157700
108898161388981614CT17INTERGENICheterozygous69275790
108898360188983604CCC4GENIChomozygous69275794
108898301088983011AG15GENIChomozygous68796746
108898513288985133AG16GENIChomozygous68452809
108898515888985159GC25GENIChomozygous68157715
108898529788985298C5GENIChomozygous69275799
108898533788985338GA9GENIChomozygous68796752
108898548888985493GAAGG11GENICheterozygous69275802
108898648688986487AG14INTERGENIChomozygous68157730
108898905688989057GA15INTERGENIChomozygous68796755
108899112288991123CT16INTERGENIChomozygous68796758
108899251788992518AT5INTERGENIChomozygous69149487
108899308088993081AG18INTERGENIChomozygous68157748
108899316088993161TC16INTERGENICheterozygous68157751
108899368188993682GA13INTERGENIChomozygous68796765
108899411788994118GA11INTERGENIChomozygous68796769
108899492988994930CT10INTERGENIChomozygous68796772
108899515788995158AG19INTERGENIChomozygous68157763
108899557688995577GT24INTERGENIChomozygous68157765
108899585788995858AG12INTERGENIChomozygous68796775
108899600388996004TC11INTERGENIChomozygous68157768
108899656888996569AG14INTERGENIChomozygous68157774
108899657588996576GA12INTERGENIChomozygous68157777
108899689588996896GT26INTERGENIChomozygous68796778
108898548888985489GA4GENIChomozygous69195214