chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47690994376909944TG33GENIChomozygous113239324
47691005476910055GA15GENIChomozygous113239326
47691012076910121GA19GENIChomozygous113239327
47691015476910155GA29GENIChomozygous113239329
47691024476910245TA38GENIChomozygous113239331
47691068076910681TG24GENIChomozygous113239332
47691083076910831CG20GENIChomozygous113239334
47691135576911356GA26GENIChomozygous113239335
47691171076911711GA20GENIChomozygous113239337
47691196176911962CA39GENIChomozygous113239339
47691200876912009GA39GENIChomozygous113239340
47691282476912825CT32GENIChomozygous113239342
47691333076913331TC23GENIChomozygous113239343
47691335276913353AG23GENIChomozygous113239345
47691356176913562AG25GENIChomozygous113239346
47691359476913595TA27GENIChomozygous113239348
47691417176914172GA27GENIChomozygous113239349
47691438176914382GA27GENIChomozygous113239351
47691466376914664TC33GENIChomozygous113239353
47691470676914707CG28GENIChomozygous113239354
47691509776915098CT24GENIChomozygous113239356
47691510876915109GA28GENIChomozygous113239357
47691515576915156GT29GENIChomozygous113239358
47691515776915158GA28GENIChomozygous113239360
47691516076915161GC26GENIChomozygous113239361
47691518376915184GA28GENIChomozygous113239363
47691523876915239CT26GENIChomozygous113239364
47691524276915243CT27GENIChomozygous113239366
47691527576915276GC22GENIChomozygous113239368