chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189829929189829930TC36GENICpossibly homozygous110172079
2189830186189830187CT27GENIChomozygous110172081
2189832570189832571AC41GENIChomozygous110172083
2189832775189832776GA29GENICpossibly homozygous110172085
2189832938189832939TC50GENICpossibly homozygous110614341
2189833916189833917AC46GENIChomozygous110172095
2189833955189833956AC42GENIChomozygous110172096
2189834787189834788AC40GENICheterozygous110172098
2189834793189834794AC39GENICheterozygous110172100