chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189909132189909133CA22GENICpossibly homozygous110805150
2189909269189909270TC22GENICheterozygous110805151
2189909684189909685TC36GENIChomozygous110172247
2189909729189909730CT28GENIChomozygous110172249
2189910256189910257CT26GENIChomozygous110172251
2189911289189911290TC29GENIChomozygous110172261