chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117574427117574427G24GENICpossibly homozygous128635892
8117574602117574603GA36GENIChomozygous116672000
8117575608117575609GA74GENIChomozygous116672002
8117576152117576153CT62GENIChomozygous116672004
8117579086117579087TC61GENIChomozygous116672006
8117580189117580190AC60GENIChomozygous116672008
8117580267117580268GA54GENIChomozygous116672010
8117574873117574874CT35GENIChomozygous116988178
8117579060117579061TC70GENIChomozygous116988179
8117579192117579193CT13GENICheterozygous132325506
8117581875117581876TC55GENIChomozygous116672012
8117582039117582044TCTAC65GENIChomozygous128635893
8117582166117582167CT62GENIChomozygous116672014
8117584809117584810AT42GENICpossibly homozygous116672016
8117590581117590582TG44GENIChomozygous116672018
8117596942117596943AC44GENIChomozygous116672022
8117597825117597826AG77GENIChomozygous116672026
8117599006117599007AG58GENIChomozygous116672028
8117599030117599031AG59GENIChomozygous116672030
8117586169117586170C52GENIChomozygous128635894
8117593787117593787ACGT30GENICheterozygous128635896
8117596175117596175T71GENIChomozygous128635897