chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185311082553110826CT15GENICheterozygous119493513
185319058953190595ATTGTA2GENIChomozygous129539073
185319793053197931TC102GENICheterozygous110351765
185320055553200556C30GENIChomozygous129539074
185320435853204358A33GENIChomozygous129539075
185320436553204367TA35GENIChomozygous129539076
185320446553204466T41GENIChomozygous129539077
185320463453204634T8GENIChomozygous129539078
185320984353209843A16GENIChomozygous129539079
185320985153209852T20GENIChomozygous129539080
185320985953209860C23GENIChomozygous129539081
185320996853209969G49GENIChomozygous129539082
185321001453210015G50GENIChomozygous129539083
185321002253210022A49GENIChomozygous129539084
185321003353210033C47GENIChomozygous129539085
185321015553210156C41GENIChomozygous129539086
185321016553210165G40GENIChomozygous129539087
185321022253210222AT53GENIChomozygous129539088
185321037353210374T37GENIChomozygous129539089
185321038053210380T37GENIChomozygous129539090
185321041653210417TC38GENIChomozygous110351777
185321042053210421CA38GENIChomozygous110351779
185321043853210439G31GENIChomozygous129539091
185321387653213876G32GENIChomozygous129539102
185321392153213921A48GENIChomozygous129539103
185322313653223137A15GENIChomozygous129539105
185322314453223145A14GENIChomozygous129539106
185322315453223155A14GENIChomozygous129539107
185323127653231277A57GENIChomozygous129539112