chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7127737979127737980TG50GENIChomozygous69101919
7127738513127738514AC41GENIChomozygous69101921
7127738922127738923AG40GENICpossibly homozygous69101923
7127739158127739159TA48GENICpossibly homozygous69101925
7127739200127739201GA45GENIChomozygous69101927
7127742052127742053GA51GENIChomozygous69101929
7127744130127744131CT45GENICpossibly homozygous69101931
7127744133127744134TC49GENIChomozygous69101933
7127744994127744995AT45GENIChomozygous69101935
7127745429127745430CT39GENIChomozygous69101937