chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2122876785122876786AG14INTERGENIChomozygous59063889
2122877088122877089TTG13INTERGENIChomozygous59063890
2122877912122877913TC8INTERGENIChomozygous59063891
2122877917122877918TTC8INTERGENIChomozygous59063892
2122877925122877926CT4INTERGENIChomozygous59063893
2122877927122877931GGGC----4INTERGENIChomozygous59063894
2122877932122877933AAT4INTERGENIChomozygous59063895
2122878891122878892TC19INTERGENIChomozygous59063896
2122879296122879297CG20INTERGENIChomozygous59063897
2122879318122879319GA16INTERGENIChomozygous59063898
2122879767122879768TA19INTERGENIChomozygous59063899
2122879884122879885TC10INTERGENIChomozygous59063900
2122880691122880692CT21INTERGENIChomozygous59063901
2122880792122880793AG20INTERGENIChomozygous59063902
2122880947122880948TC15INTERGENIChomozygous59063903
2122881233122881234TG14INTERGENIChomozygous59063904
2122881461122881462CT11INTERGENIChomozygous59063905
2122881887122881888AG14INTERGENIChomozygous59063906
2122882028122882029GA16INTERGENIChomozygous59063907
2122882047122882048CT16INTERGENIChomozygous59063908
2122882500122882501TC15INTERGENIChomozygous59063909
2122882683122882689TGTGTG------6INTERGENIChomozygous59063910
2122882746122882747AG12INTERGENIChomozygous59063911
2122882921122882922GA14INTERGENIChomozygous59063912
2122882954122882955CA12INTERGENIChomozygous59063913
2122883558122883559GC14INTERGENIChomozygous59063914
2122884012122884013TA26INTERGENIChomozygous59063915
2122884081122884082AT13INTERGENIChomozygous59063916