chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2122876785122876786AG2INTERGENIChomozygous59063889
2122877088122877089TTG6INTERGENIChomozygous59063890
2122877912122877913TC9INTERGENIChomozygous59063891
2122877917122877918TTC9INTERGENIChomozygous59063892
2122877925122877926CT9INTERGENIChomozygous59063893
2122877927122877931GGGC----9INTERGENIChomozygous59063894
2122877932122877933AAT9INTERGENIChomozygous59063895
2122878891122878892TC14INTERGENIChomozygous59063896
2122879296122879297CG9INTERGENIChomozygous59063897
2122879318122879319GA6INTERGENIChomozygous59063898
2122879767122879768TA6INTERGENIChomozygous59063899
2122879884122879885TC15INTERGENIChomozygous59063900
2122880691122880692CT13INTERGENIChomozygous59063901
2122880792122880793AG8INTERGENIChomozygous59063902
2122880947122880948TC15INTERGENIChomozygous59063903
2122881233122881234TG13INTERGENIChomozygous59063904
2122881461122881462CT9INTERGENIChomozygous59063905
2122881887122881888AG5INTERGENIChomozygous59063906
2122882028122882029GA14INTERGENIChomozygous59063907
2122882047122882048CT13INTERGENIChomozygous59063908
2122882500122882501TC13INTERGENIChomozygous59063909
2122882683122882689TGTGTG------9INTERGENIChomozygous59063910
2122882746122882747AG17INTERGENIChomozygous59063911
2122882921122882922GA7INTERGENIChomozygous59063912
2122882954122882955CA11INTERGENIChomozygous59063913
2122883558122883559GC16INTERGENIChomozygous59063914
2122884012122884013TA5INTERGENIChomozygous59063915
2122884081122884082AT2INTERGENIChomozygous59063916