chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173126315831263159GC18GENIChomozygous111025420
173126316031263161TG18GENIChomozygous111025422
173127758331277584G9GENIChomozygous130463017
173127759431277595C10GENIChomozygous130463018
173127760131277602A12GENIChomozygous130463019
173127762131277623GG15GENIChomozygous130463020
173127763131277631A17GENIChomozygous130463021
173127763431277638GAGT17GENIChomozygous130463022
173127765131277652C22GENIChomozygous130463023
173127765631277656G22GENIChomozygous130463024
173127766831277669G25GENIChomozygous130463025
173128724331287244C17GENIChomozygous129442713
173132497231324973C1GENIChomozygous129442726
173132497731324977T2GENIChomozygous129442727
173132507731325077A3GENIChomozygous129442728
173134593931345939GGC13GENIChomozygous129442744
173134609931346100A19GENIChomozygous129442745
173134813531348135A26GENIChomozygous129442748
173135003931350039CCGTT6GENIChomozygous129442752
173127752431277528TTGT1GENIChomozygous130706993
173127754931277550G4GENIChomozygous132215304
173132857331328574C9GENICheterozygous132215307
173127761731277618AG15GENIChomozygous130467389
173127761831277619CA15GENIChomozygous130467390