chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5137271429137271430GA26GENIChomozygous114536404
5137273611137273612GA38GENICpossibly homozygous114536406
5137274112137274113CT23GENIChomozygous114443898
5137277934137277935GT7GENIChomozygous114536410
5137281610137281611AG17GENIChomozygous114022661
5137281760137281761CA21GENIChomozygous114536412