chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6137118710137118711CT33GENICpossibly homozygous114996652
6137119884137119885CT21GENIChomozygous114996653
6137120154137120155CA50GENICheterozygous114996654
6137121043137121044CA23GENIChomozygous114996655
6137122371137122372AG36GENIChomozygous114996656
6137122593137122594CT36GENIChomozygous114996657