chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104890468048904681CT16GENIChomozygous116881129
104890511748905118GT13GENICheterozygous116881131
104890512148905122GT13GENICheterozygous116881133
104890567748905678AG18GENIChomozygous116881135
104890581848905819CT13GENIChomozygous116881137
104890752348907524CT18GENIChomozygous116881139
104890804348908044TG8GENIChomozygous116881141
104890811848908119CG18GENIChomozygous116881143
104890824048908241AG12GENIChomozygous116881145
104890863148908632TC27GENIChomozygous116881147
104890870948908710TC16GENIChomozygous116881149
104890891648908917TG17GENIChomozygous116881151
104890930148909302GA4GENIChomozygous116881153
104890960148909602TC7GENIChomozygous116881155
104890970848909709CT11GENIChomozygous116881157
104891076148910762TC15GENIChomozygous116881161
104891187448911875CT18GENIChomozygous116881163
104891246548912466GA22GENIChomozygous116881165
104891254648912547CT15GENIChomozygous116881167
104891329148913292TC4GENIChomozygous116881171
104891368548913686CG8GENIChomozygous116881173
104891369548913696GT15GENIChomozygous116881175
104891386248913863CA19GENIChomozygous116881177
104891410148914102GC19GENIChomozygous116881179
104891447648914477CT16GENIChomozygous116881181
104891481148914812CT20GENIChomozygous116881183
104891498748914988TC10GENIChomozygous116881185
104891511348915114CA21GENIChomozygous116881187
104891590848915909GA11GENIChomozygous116881189
104891776948917770AG10GENIChomozygous116881191
104891854448918545AG14GENIChomozygous116881193
104891876848918769TC19GENIChomozygous116881195
104892011148920112GA5GENIChomozygous118036966
104892084448920845CG16GENIChomozygous117078212
104892203148922032TC19GENIChomozygous116881197
104892312348923124TC10GENIChomozygous116881199
104892331248923313AG5GENIChomozygous116881201
104892359548923596CT10GENIChomozygous116881203
104892499948925000GA10GENIChomozygous116881207