chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47690994376909944TG22GENIChomozygous113239324
47691005476910055GA24GENIChomozygous113239326
47691012076910121GA23GENIChomozygous113239327
47691015476910155GA21GENIChomozygous113239329
47691068076910681TG21GENIChomozygous113239332
47691083076910831CG25GENIChomozygous113239334
47691135576911356GA39GENIChomozygous113239335
47691171076911711GA29GENIChomozygous113239337
47691196176911962CA36GENIChomozygous113239339
47691200876912009GA35GENIChomozygous113239340
47691282476912825CT17GENIChomozygous113239342
47691333076913331TC26GENIChomozygous113239343
47691335276913353AG26GENIChomozygous113239345
47691356176913562AG24GENIChomozygous113239346
47691359476913595TA26GENIChomozygous113239348
47691417176914172GA23GENIChomozygous113239349
47691438176914382GA20GENIChomozygous113239351
47691466376914664TC23GENIChomozygous113239353
47691470676914707CG22GENIChomozygous113239354
47691509776915098CT35GENIChomozygous113239356
47691510876915109GA38GENIChomozygous113239357
47691515576915156GT39GENIChomozygous113239358
47691515776915158GA40GENIChomozygous113239360
47691516076915161GC39GENIChomozygous113239361
47691518376915184GA39GENIChomozygous113239363
47691523876915239CT41GENIChomozygous113239364
47691524276915243CT42GENIChomozygous113239366
47691527576915276GC26GENIChomozygous113239368