chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155082449750824498AAG5GENIChomozygous49052480
155085438950854391GT--9GENICheterozygous49149183
155088608150886082C-27GENIChomozygous48306079
155088609250886094AC--26GENIChomozygous48306080
155088610250886103GGC27GENIChomozygous48306081
155088907150889072GGA20GENICheterozygous48306087
155088978950889790CCTTTTTT22GENICheterozygous49052487
155089964450899646GT--4GENICheterozygous48671792
155091716350917164TG12GENIChomozygous48306115
155091717950917180TG8GENIChomozygous48306117
155092249350922494TC21GENIChomozygous48306129
155092249750922498CT24GENIChomozygous48306130
155092249850922499AT24GENIChomozygous48306131
155092618150926185CACT----5GENICheterozygous49052489
155092843250928433GT28GENIChomozygous48306138
155092843850928439AC29GENIChomozygous48306139