chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2122876785122876786AG13INTERGENIChomozygous59063889
2122877088122877089TTG15INTERGENIChomozygous59063890
2122877912122877913TC5INTERGENICheterozygous59063891
2122877917122877918TTC2INTERGENIChomozygous59063892
2122877925122877926CT1INTERGENIChomozygous59063893
2122877927122877931GGGC----1INTERGENIChomozygous59063894
2122877932122877933AAT1INTERGENIChomozygous59063895
2122878891122878892TC14INTERGENIChomozygous59063896
2122879296122879297CG5INTERGENIChomozygous59063897
2122879318122879319GA6INTERGENIChomozygous59063898
2122879767122879768TA8INTERGENIChomozygous59063899
2122879884122879885TC21INTERGENIChomozygous59063900
2122880691122880692CT24INTERGENIChomozygous59063901
2122880792122880793AG18INTERGENIChomozygous59063902
2122880947122880948TC13INTERGENIChomozygous59063903
2122881233122881234TG21INTERGENIChomozygous59063904
2122881461122881462CT7INTERGENIChomozygous59063905
2122881887122881888AG12INTERGENIChomozygous59063906
2122882028122882029GA18INTERGENIChomozygous59063907
2122882047122882048CT16INTERGENIChomozygous59063908
2122882500122882501TC19INTERGENIChomozygous59063909
2122882746122882747AG12INTERGENIChomozygous59063911
2122882921122882922GA16INTERGENIChomozygous59063912
2122882954122882955CA20INTERGENIChomozygous59063913
2122883558122883559GC7INTERGENIChomozygous59063914
2122884012122884013TA3INTERGENIChomozygous59063915
2122884081122884082AT4INTERGENICheterozygous59063916