chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104890468048904681CT33GENIChomozygous116881129
104890511748905118GT41GENIChomozygous116881131
104890512148905122GT39GENIChomozygous116881133
104890567748905678AG34GENIChomozygous116881135
104890581848905819CT35GENIChomozygous116881137
104890752348907524CT41GENIChomozygous116881139
104890804348908044TG37GENIChomozygous116881141
104890811848908119CG42GENIChomozygous116881143
104890824048908241AG40GENIChomozygous116881145
104890863148908632TC32GENIChomozygous116881147
104890870948908710TC41GENIChomozygous116881149
104890891648908917TG39GENIChomozygous116881151
104890930148909302GA36GENIChomozygous116881153
104890960148909602TC21GENIChomozygous116881155
104890970848909709CT24GENIChomozygous116881157
104891006948910070GA32GENIChomozygous116881159
104891076148910762TC33GENIChomozygous116881161
104891187448911875CT49GENIChomozygous116881163
104891246548912466GA20GENIChomozygous116881165
104891254648912547CT37GENIChomozygous116881167
104891327048913271GA30GENIChomozygous116881169
104891329148913292TC31GENIChomozygous116881171
104891368548913686CG31GENIChomozygous116881173
104891369548913696GT36GENIChomozygous116881175
104891386248913863CA28GENIChomozygous116881177
104891410148914102GC27GENIChomozygous116881179
104891447648914477CT30GENIChomozygous116881181
104891481148914812CT31GENIChomozygous116881183
104891498748914988TC47GENIChomozygous116881185
104891511348915114CA28GENIChomozygous116881187
104891590848915909GA29GENICpossibly homozygous116881189
104891665248916653CT20GENICheterozygous118036963
104891682448916825CT21GENICheterozygous118102905
104891776948917770AG17GENIChomozygous116881191
104891854448918545AG32GENIChomozygous116881193
104891876848918769TC21GENIChomozygous116881195
104891971848919719AG39GENIChomozygous118036965
104892011148920112GA27GENICheterozygous118036966
104892084448920845CG29GENIChomozygous117078212
104892203148922032TC23GENIChomozygous116881197
104892312348923124TC42GENICpossibly homozygous116881199
104892331248923313AG22GENIChomozygous116881201
104892359548923596CT36GENICpossibly homozygous116881203
104892499948925000GA39GENIChomozygous116881207