chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1217602995217602996TA17GENIChomozygous125308764
1217603209217603210CT8GENIChomozygous125438807
1217603553217603554CA16GENIChomozygous125378379
1217603596217603597AG9GENIChomozygous125308766
1217606187217606188TG15GENIChomozygous125308771
1217606931217606932AG10GENIChomozygous125378380
1217607738217607739AG21GENIChomozygous125308773
1217609252217609253GA7GENIChomozygous125438808
1217609953217609954CT18GENIChomozygous125308774
1217611091217611092CG28GENIChomozygous125378381
1217611852217611853CT11GENIChomozygous125378382
1217612218217612219CT13GENIChomozygous125308775
1217612364217612365GA14GENIChomozygous125378383
1217612879217612880TG8GENIChomozygous125308777
1217613863217613864CT14GENIChomozygous125308779
1217615509217615510AC10GENIChomozygous125308780
1217616386217616387AG21GENIChomozygous125308781
1217618053217618054GA13GENIChomozygous125378384
1217619082217619083GA18GENIChomozygous125378385
1217624409217624410AG17GENIChomozygous125308786
1217625574217625575CT10GENIChomozygous125378387
1217626284217626285GA23GENIChomozygous125378388
1217626376217626377AG14GENIChomozygous125308787
1217630483217630484AC22GENIChomozygous125378389
1217635781217635782TC10GENIChomozygous125378390
1217635825217635826CT9GENIChomozygous125378391
1217636899217636900TC9GENICheterozygous125308794