chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145118105145118106G37GENICpossibly homozygous128087891
4145121086145121087CT50GENIChomozygous112870632
4145119403145119404TA40GENIChomozygous112870628
4145119523145119524GC47GENIChomozygous112870629
4145119998145119999TC51GENIChomozygous112870630
4145121025145121026CT37GENIChomozygous112870631
4145121377145121378GA38GENIChomozygous112870633
4145123158145123159TC76GENIChomozygous112870634
4145123623145123624GT56GENIChomozygous112870635
4145124114145124115AG33GENIChomozygous112870636
4145125355145125356T44GENIChomozygous128087892
4145125862145125863A42GENIChomozygous128087893
4145125968145125969CT49GENIChomozygous112870637
4145126827145126828CT74GENIChomozygous112870638
4145127424145127425A47GENIChomozygous128087894
4145127578145127578A48GENIChomozygous128087895
4145127769145127770GT19GENIChomozygous112870639
4145128121145128122AC21GENIChomozygous126024896
4145134090145134091AG4GENIChomozygous126024902
4145134176145134176T5GENIChomozygous128087896
4145134350145134351CT21GENIChomozygous126024903
4145135353145135354C28GENIChomozygous128087897
4145135367145135367G26GENIChomozygous128087898
4145135378145135380GC26GENIChomozygous128087899
4145135390145135391A23GENIChomozygous128087900
4145142820145142821AG32GENIChomozygous112870640
4145143496145143500CTCA9GENIChomozygous128087901
4145145654145145654C50GENICpossibly homozygous128087902
4145146498145146499AG28GENIChomozygous112870642
4145124187145124187TG10GENIChomozygous132060111
4145135447145135448AC5GENIChomozygous129910809
4145135458145135459A5GENIChomozygous129904589