chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25267898252678983CG32GENICpossibly homozygous140979314
25269311452693115A11GENICheterozygous403002101
25269311452693115AT11GENICheterozygous403002102
25271838452718385A31GENICheterozygous135907299
25274168052741681TC15GENICheterozygous153924621
25274168052741681T15GENICheterozygous404056022
25275021252750213T22GENICheterozygous140968807
25280151352801514C18GENICheterozygous403002135
25280151352801514CT18GENICheterozygous403002136
25280151452801515C18GENICheterozygous403002137
25280151452801515CT18GENICheterozygous403002138
25280151552801516CT21GENICheterozygous403002139
25280151552801516C21GENICheterozygous403002140