chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185311084253110842A18GENICheterozygous132510255
185319058953190595ATTGTA4GENIChomozygous129539073
185319793053197931TC99GENICheterozygous110351765
185320055553200556C37GENIChomozygous129539074
185320435853204358A35GENIChomozygous129539075
185320436553204367TA32GENIChomozygous129539076
185320446553204466T40GENIChomozygous129539077
185320463453204634T4GENIChomozygous129539078
185320984353209843A14GENIChomozygous129539079
185320985153209852T17GENIChomozygous129539080
185320985953209860C18GENIChomozygous129539081
185320996853209969G47GENIChomozygous129539082
185321001453210015G51GENIChomozygous129539083
185321002253210022A51GENIChomozygous129539084
185321003353210033C45GENIChomozygous129539085
185321015553210156C50GENIChomozygous129539086
185321016553210165G47GENIChomozygous129539087
185321022253210222AT47GENIChomozygous129539088
185321037353210374T31GENIChomozygous129539089
185321038053210380T33GENIChomozygous129539090
185321041653210417TC31GENIChomozygous110351777
185321042053210421CA31GENIChomozygous110351779
185321043853210439G24GENIChomozygous129539091
185321387653213876G38GENIChomozygous129539102
185321392153213921A44GENIChomozygous129539103
185322313653223137A14GENIChomozygous129539105
185322314453223145A14GENIChomozygous129539106
185322315453223155A13GENIChomozygous129539107
185323127653231277A66GENIChomozygous129539112