| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66002065-66002848 | Common:4; Rare:221; Clinvar:8; Clinvar (benign):3 | ||||
| chr11:66011340-66011491 | Common:1; Rare:16 | ||||
| chr11:66011869-66012017 | Rare:38 | ||||
| chr11:66021128-66021285 | Rare:42 | ||||
| chr11:66045120-66045420 | Common:4; Rare:86 | ||||
| chr11:66051978-66052412 | Common:6; Rare:129 | ||||
| chr11:66070149-66070381 | Common:1; Rare:83 | ||||
| chr11:66257462-66257678 | Rare:54 | ||||
| chr11:66257870-66258120 | Common:2; Rare:56 | ||||
| chr11:66268113-66268254 | Common:2; Rare:25 | ||||
| chr11:66268325-66268653 | Common:3; Rare:92 | ||||
| chr11:66268750-66268908 | Common:2; Rare:44 | ||||
| chr11:66289073-66289467 | Common:1; Rare:99 | ||||
| chr11:66291791-66291901 | Rare:25 | ||||
| chr11:66336398-66336540 | Rare:36 |