| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67428333-67428509 | Rare:51 | ||||
| chr11:67443456-67443587 | Common:1; Rare:44 | ||||
| chr11:67443756-67443899 | Rare:35 | ||||
| chr11:67464635-67464864 | Rare:134 | ||||
| chr11:67469133-67469444 | Common:3; Rare:106 | ||||
| chr11:67482853-67483055 | Common:1; Rare:48; Clinvar (pathogenic):1 | ||||
| chr11:67483259-67483582 | Common:1; Rare:92 | ||||
| chr11:67504320-67504710 | Common:2; Rare:94 | ||||
| chr11:67505311-67505452 | Rare:36 | ||||
| chr11:67508156-67508326 | Common:1; Rare:37 | ||||
| chr11:67508678-67508796 | Common:2; Rare:49 | ||||
| chr11:67583542-67583874 | Common:2; Rare:101 | ||||
| chr11:67584038-67584438 | Common:9; Rare:155 | ||||
| chr11:67606722-67606968 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68010697-68011097 | Common:3; Rare:112 |