chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2122876785122876786AG8INTERGENICpossibly homozygous59063889
2122877088122877089TTG13INTERGENIChomozygous59063890
2122877912122877913TC4INTERGENICheterozygous59063891
2122877917122877918TTC3INTERGENICheterozygous59063892
2122877925122877926CT1INTERGENIChomozygous59063893
2122877927122877931GGGC----1INTERGENIChomozygous59063894
2122877932122877933AAT2INTERGENIChomozygous59063895
2122878891122878892TC19INTERGENIChomozygous59063896
2122879296122879297CG7INTERGENIChomozygous59063897
2122879318122879319GA12INTERGENIChomozygous59063898
2122879767122879768TA15INTERGENIChomozygous59063899
2122879884122879885TC19INTERGENIChomozygous59063900
2122880691122880692CT20INTERGENIChomozygous59063901
2122880792122880793AG18INTERGENICheterozygous59063902
2122880947122880948TC23INTERGENIChomozygous59063903
2122881233122881234TG27INTERGENIChomozygous59063904
2122881461122881462CT7INTERGENIChomozygous59063905
2122881887122881888AG17INTERGENIChomozygous59063906
2122882028122882029GA7INTERGENIChomozygous59063907
2122882047122882048CT15INTERGENIChomozygous59063908
2122882500122882501TC20INTERGENIChomozygous59063909
2122882746122882747AG18INTERGENICpossibly homozygous59063911
2122882921122882922GA21INTERGENIChomozygous59063912
2122882954122882955CA27INTERGENIChomozygous59063913
2122883558122883559GC9INTERGENICheterozygous59063914
2122884012122884013TA14INTERGENICpossibly homozygous59063915
2122884081122884082AT15INTERGENICheterozygous59063916