chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7127737979127737980TG7GENIChomozygous69101919
7127738513127738514AC16GENIChomozygous69101921
7127738922127738923AG12GENIChomozygous69101923
7127739200127739201GA12GENIChomozygous69101927
7127742052127742053GA5GENIChomozygous69101929
7127739063127739064CA9GENIChomozygous69794448
7127741352127741353CT13GENIChomozygous69381898
7127743429127743430GA5GENIChomozygous69933942
7127744130127744131CT9GENIChomozygous69101931
7127744133127744134TC9GENIChomozygous69101933
7127744994127744995AT17GENIChomozygous69101935
7127745457127745458GA7GENICpossibly homozygous69933944