chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117574873117574874CT8GENIChomozygous116988178
8117575809117575810GA15GENIChomozygous117920311
8117575810117575811TG15GENIChomozygous117920312
8117576474117576475GT5GENICheterozygous123100597
8117576476117576477CT7GENICheterozygous134095711
8117576477117576478CT7GENICheterozygous134095712
8117576480117576481AT7GENICheterozygous134095713
8117577202117577203TC8GENICpossibly homozygous117125072
8117578543117578544T14GENIChomozygous131054379
8117578708117578709CT4GENIChomozygous117149575
8117579060117579061TC12GENIChomozygous116988179
8117579086117579087TC9GENIChomozygous116672006
8117579724117579725GA7GENIChomozygous117149577
8117580189117580190AC13GENIChomozygous116672008
8117580838117580839GT15GENIChomozygous117149578
8117581875117581876TC17GENIChomozygous116672012
8117585480117585481CA9GENIChomozygous117125087
8117585495117585496GA8GENIChomozygous117149579
8117586169117586170C11GENIChomozygous128635894
8117590331117590332TC15GENIChomozygous117149580
8117590581117590582TG7GENIChomozygous116672018
8117596914117596915CT12GENIChomozygous117149581
8117596942117596943AC13GENIChomozygous116672022
8117597137117597137G18GENIChomozygous131054382
8117597825117597826AG13GENIChomozygous116672026
8117599006117599007AG14GENIChomozygous116672028
8117599030117599031AG17GENIChomozygous116672030