chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106377610663776107GC3GENIChomozygous786335165
106377622363776224AG16GENIChomozygous786335166
106377820363778204CA21GENIChomozygous786335167
106377983363779834GT9GENIChomozygous786335168
106377986863779869AC10GENIChomozygous786335169
106378004863780049GT16GENIChomozygous786335170
106378039763780398AC10GENIChomozygous786335171
106378056363780564GT12GENIChomozygous786335172
106378074563780746AT11GENIChomozygous786335173
106378078263780783CT13GENIChomozygous786335174
106378083663780837GA4GENIChomozygous786335175
106378104263781043CG8GENIChomozygous786335176
106378119563781196CG4GENIChomozygous786335177
106378120663781207GT13GENIChomozygous786335178
106378136063781361AC8GENIChomozygous786335179
106378148363781484GT21GENIChomozygous786335180
106378207463782075TC31GENIChomozygous786335181
106378294663782947CT18GENIChomozygous786335182
106378403763784038CG22GENIChomozygous786335183
106378473463784735AT22GENIChomozygous786335184
106378485563784856GA19GENIChomozygous786335185
106378802363788024CT20GENICpossibly homozygous786335186
106378870963788710GC23GENICheterozygous786335187
106378928963789290TC24GENIChomozygous786335188
106378943963789440GT24GENIChomozygous786335189
106379062063790621AC11GENIChomozygous786335190
106379067163790672TC16GENIChomozygous786335191
106379087663790877AG21GENIChomozygous786335192
106379279063792791CT18GENIChomozygous786335193
106379419263794193CT15GENIChomozygous786335194
106379419663794197CT15GENIChomozygous786335195
106379420863794209TC14GENIChomozygous786335196
106379443963794440TC12GENIChomozygous786335197
106379444063794441TC12GENIChomozygous786335198
106379449263794493AC15GENIChomozygous786335199
106379451963794520GC14GENIChomozygous786335200
106379453263794533GC20GENIChomozygous786335201
106379466163794662GT26GENIChomozygous786335202
106379474163794742GC26GENIChomozygous786335203
106379501463795015TC19GENIChomozygous786335204