chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135282103852821039CT59GENICpossibly homozygous776959382
135282118652821187GA42GENIChomozygous776959383
135282119552821196GT34GENIChomozygous776959384
135282119652821197CT34GENIChomozygous776959385
135282122852821229AT36GENIChomozygous776959386
135282141452821415GA43GENIChomozygous776959387
135282153652821537CT62GENIChomozygous776959388
135282185252821853GA43GENICpossibly homozygous776959389
135282215952822160CT61GENIChomozygous776959390
135282253752822538GA62GENIChomozygous776959391
135282264152822642TC37GENIChomozygous776959392
135282275652822757GC37GENIChomozygous776959393
135282291552822916AG45GENIChomozygous776959394
135282292252822923GA40GENIChomozygous776959395