chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2122876785122876786AG18INTERGENIChomozygous59063889
2122877088122877089TTG18INTERGENICheterozygous59063890
2122877095122877096GGA21INTERGENICheterozygous60753475
2122877912122877913TC15INTERGENIChomozygous59063891
2122877917122877918TTC16INTERGENIChomozygous59063892
2122877925122877926CT18INTERGENIChomozygous59063893
2122877927122877931GGGC----22INTERGENIChomozygous59063894
2122877932122877933AAT18INTERGENIChomozygous59063895
2122878657122878658T-8INTERGENICheterozygous60496126
2122878891122878892TC21INTERGENIChomozygous59063896
2122879296122879297CG28INTERGENIChomozygous59063897
2122879318122879319GA26INTERGENIChomozygous59063898
2122879767122879768TA22INTERGENIChomozygous59063899
2122879884122879885TC21INTERGENIChomozygous59063900
2122880691122880692CT22INTERGENIChomozygous59063901
2122880792122880793AG22INTERGENIChomozygous59063902
2122880947122880948TC17INTERGENIChomozygous59063903
2122881233122881234TG29INTERGENIChomozygous59063904
2122881461122881462CT20INTERGENICpossibly homozygous59063905
2122881887122881888AG21INTERGENIChomozygous59063906
2122882028122882029GA25INTERGENIChomozygous59063907
2122882047122882048CT21INTERGENIChomozygous59063908
2122882500122882501TC25INTERGENIChomozygous59063909
2122882683122882689TGTGTG------13INTERGENIChomozygous59063910
2122882746122882747AG14INTERGENIChomozygous59063911
2122882921122882922GA25INTERGENIChomozygous59063912
2122882954122882955CA26INTERGENIChomozygous59063913
2122883558122883559GC27INTERGENIChomozygous59063914
2122884012122884013TA15INTERGENIChomozygous59063915
2122884081122884082AT13INTERGENIChomozygous59063916