chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5133989913133989914TC10GENIChomozygous114015239
5133990589133990590TC21GENIChomozygous114015240
5133991146133991147TC19GENIChomozygous114015241
5133993265133993266TG12GENIChomozygous114015245
5133994807133994808GA10GENIChomozygous114015247
5133994934133994935TC18GENIChomozygous114532401
5133994935133994936CT18GENIChomozygous118943407
5133995985133995986TC29GENIChomozygous114015251
5133996535133996536GC13GENIChomozygous114015252
5134002244134002245AG20GENIChomozygous114015263
5134002993134002994CG28GENIChomozygous114015264
5134005046134005047CT14GENIChomozygous114015265
5134005868134005869TC18GENIChomozygous114015266
5134006730134006731GA23GENIChomozygous114015267
5134007807134007808AG15GENIChomozygous114015268
5134007872134007873TA15GENIChomozygous114015269
5134007877134007878GA17GENIChomozygous114015270
5134008148134008149AG16GENIChomozygous114015271
5134008165134008166GC13GENIChomozygous114015272
5134008209134008210GA15GENIChomozygous114015273