chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189829637189829638AG14GENIChomozygous802169155
2189829929189829930TC13GENIChomozygous802169156
2189829990189829991CT17GENIChomozygous802169157
2189830864189830865AG16GENICheterozygous802169158
2189831648189831649CA21GENIChomozygous802169159
2189832666189832667GA24GENICpossibly homozygous802169160
2189833916189833917AC15GENICpossibly homozygous802169161
2189834736189834737AG23GENICpossibly homozygous802169162
2189835091189835092TA18GENIChomozygous802169163