chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185311876453118765A35GENICheterozygous132227321
185319793053197931TC91GENICheterozygous110351765
185320055553200556C33GENIChomozygous129539074
185320435853204358A42GENIChomozygous129539075
185320436553204367TA45GENIChomozygous129539076
185320446553204466T42GENIChomozygous129539077
185320463453204634T6GENIChomozygous129539078
185320984353209843A10GENIChomozygous129539079
185320985153209852T13GENIChomozygous129539080
185320985953209860C17GENIChomozygous129539081
185320996853209969G49GENIChomozygous129539082
185321001453210015G43GENIChomozygous129539083
185321002253210022A45GENIChomozygous129539084
185321003353210033C44GENIChomozygous129539085
185321015553210156C51GENIChomozygous129539086
185321016553210165G50GENIChomozygous129539087
185321022253210222AT49GENIChomozygous129539088
185321037353210374T36GENIChomozygous129539089
185321038053210380T37GENIChomozygous129539090
185321041653210417TC31GENIChomozygous110351777
185321042053210421CA31GENIChomozygous110351779
185321043853210439G27GENIChomozygous129539091
185316558753165588TG46GENICpossibly homozygous132231168
185321387653213876G26GENIChomozygous129539102
185321392153213921A39GENIChomozygous129539103
185322313653223137A18GENIChomozygous129539105
185322314453223145A18GENIChomozygous129539106
185322315453223155A18GENIChomozygous129539107
185323127653231277A56GENIChomozygous129539112