chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207867257207867258GA18GENIChomozygous59931777
2207867837207867838CCAG11GENICheterozygous59931778
2207871200207871201AG12GENIChomozygous59356626
2207871595207871596GGCCTGGCT24GENIChomozygous59356627
2207872469207872470GGTTTGTTT15GENIChomozygous59356630
2207873609207873610CCT12GENICpossibly homozygous59931781