chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8113565452113565453CG-1GENIC180768166
8113565458113565459AG-1GENIC180768167
8113566751113566752GA-1GENIC183277179
8113567371113567372TC-1GENIC183277180
8113570193113570194TA-1GENIC183277181
8113570440113570441TC-1GENIC183277182
8113579247113579248CT-1GENIC183277183
8113581904113581905GA-1GENIC183277184
8113582208113582209GT-1GENIC183277185
8113586812113586813AT-1GENIC183277186
8113586939113586940CA-1GENIC180768168
8113587025113587026CG-1GENIC183277187
8113587032113587033CT-1GENIC180768169
8113587076113587077CA-1GENIC183277188
8113587092113587093CA-1GENIC180768170
8113587193113587194GT-1GENIC180768171
8113587623113587624TG-1GENIC183277189
8113587624113587625TG-1GENIC183277190
8113588621113588622AG-1GENIC180768172
8113589207113589208GA-1GENIC183277191
8113591456113591457CT-1GENIC183277192
8113594146113594147AT-1GENIC183277193
8113594267113594268TC-1GENIC183277194
8113594721113594722TC-1GENIC183277195
8113595056113595057CA-1GENIC183277196
8113595097113595098GT-1GENIC183277197
8113596421113596422AT-1GENIC180768173
8113597908113597909TG-1GENIC180768174
8113599212113599213GT-1GENIC183277198
8113600322113600323AG-1GENIC180768175
8113603416113603417TC-1GENIC183277199
8113603423113603424GC-1GENIC183277200
8113603913113603914AC-1GENIC180768176
8113604182113604183GT-1GENIC183277201