chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123941568139415682AG24GENIChomozygous50199117
123941621539416216TTG14GENICheterozygous50199119
123941621739416218T-14GENICheterozygous50199121
123941622239416223G-14GENIChomozygous50199123
123941622239416223GGTGTGTGT1GENIChomozygous50199125
123941624839416249AT14GENICpossibly homozygous50199129
123941675139416752CT12GENICheterozygous50451963
123941681439416815TTC4GENICheterozygous50199135
123941681939416820TTCC3GENICheterozygous50199137
123941691739416918TTC1GENIChomozygous50199139
123941715539417156C-8GENIChomozygous50199143
123941717039417172AA--6GENICheterozygous50199145
123941720339417204C-7GENIChomozygous50199147
123941749539417507TATTATTATTAT------------2GENIChomozygous50199149
123941773239417733TC26GENIChomozygous50199151
123941773639417737AG26GENIChomozygous50199153
123941777039417771CG36GENIChomozygous50199155
123941782539417826GC36GENIChomozygous50199157
123941787239417873CG37GENIChomozygous50199159
123941843639418438GA--11GENICheterozygous50199161
123941843939418445TGATTG------11GENICheterozygous50199163
123941955139419552CT23GENIChomozygous50199167
123941974739419748CT19GENIChomozygous50199169
123942085039420851CCTTT4GENIChomozygous50199171
123942120839421209AG15GENIChomozygous50199173
123942347639423477CCT12GENICheterozygous50199177
123942356039423562AA--5GENICheterozygous50199179
123942361739423618TTC1GENIChomozygous50199183
123942401339424014C-12GENICheterozygous50199185
123942401439424015T-5GENICheterozygous50199187
123942417239424176ACAC----4GENIChomozygous50199189
123942448439424485TTC24GENIChomozygous50199191
123942492939424930AG24GENIChomozygous50199193
123942548839425489CCT21GENIChomozygous50199195
123942549539425496TC17GENIChomozygous50199197
123942626139426262AT23GENIChomozygous50199199
123942652839426529CT24GENIChomozygous50199201