chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4176510144176510145TC16INTERGENICpossibly homozygous57854916
4176511647176511648GC12INTERGENICheterozygous57854917
4176511744176511745CCT11INTERGENICpossibly homozygous57854918
4176511795176511796GT22INTERGENIChomozygous57854919
4176512186176512187GA17INTERGENIChomozygous57854920
4176512419176512420TG6INTERGENIChomozygous57854921
4176512517176512518TC8INTERGENIChomozygous57854922
4176512555176512556AG6INTERGENIChomozygous57854923
4176512987176512988AG21INTERGENICpossibly homozygous57854924
4176513560176513561CT20INTERGENICpossibly homozygous57854925
4176513740176513741GC13INTERGENIChomozygous57854926
4176513832176513833AC8INTERGENIChomozygous57854927
4176513960176513961AC17INTERGENIChomozygous57854928
4176514170176514173AGT---6INTERGENIChomozygous57854929
4176514666176514667GGA19INTERGENIChomozygous57854930
4176515443176515444T-12INTERGENICpossibly homozygous57854931
4176515472176515473CT26INTERGENICpossibly homozygous57854932
4176515684176515685CT13INTERGENIChomozygous57854933
4176515691176515692TA11INTERGENIChomozygous57854934
4176516114176516115AG13INTERGENIChomozygous57854935
4176517029176517030CA15INTERGENICpossibly homozygous57854936
4176517745176517746TA15INTERGENIChomozygous57854937