chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7127737979127737980TG38GENICpossibly homozygous69101919
7127738513127738514AC35GENIChomozygous69101921
7127738922127738923AG20GENIChomozygous69101923
7127739059127739060CA17GENICheterozygous69862316
7127739063127739064CA15GENICpossibly homozygous69794448
7127739200127739201GA34GENIChomozygous69101927
7127742052127742053GA23GENIChomozygous69101929
7127743480127743481AG8GENICheterozygous69862317
7127744130127744131CT20GENIChomozygous69101931
7127744133127744134TC21GENIChomozygous69101933
7127741352127741353CT20GENIChomozygous69381898