chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4697896546978966GT14GENIChomozygous792108138
X4698047346980474GA13GENIChomozygous792108139
X4699030346990304CT4GENIChomozygous792108140
X4699293446992935AG5GENIChomozygous792108141
X4699487146994872CT8GENIChomozygous792108142
X4699539946995400AC3GENIChomozygous792108143
X4699556346995564CT10GENIChomozygous792108144
X4699656146996562TC8GENIChomozygous792108145
X4699661846996619GA13GENICheterozygous792108146
X4700354147003542TA4GENIChomozygous792108147
X4700358147003582CT4GENIChomozygous792108148
X4700365247003653CA5GENIChomozygous792108149
X4700435447004355CT6GENIChomozygous792108150
X4700842547008426GA6GENIChomozygous792108151
X4700983947009840AG6GENIChomozygous792108152
X4701146647011467AG9GENIChomozygous792108153
X4701181447011815CT7GENIChomozygous792108154
X4701302747013028CT7GENIChomozygous792108155
X4701486347014864AC9GENIChomozygous792108156
X4701660847016609AG8GENIChomozygous792108157
X4701675447016755TA5GENIChomozygous792108158
X4702029747020298TC6GENIChomozygous792108159
X4702521947025220CT13GENIChomozygous792108160
X4702589247025893TC9GENIChomozygous792108161