| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65575855-65576054 | Common:3; Rare:59 | ||||
| chr11:65614071-65614335 | Rare:63 | ||||
| chr11:65638082-65638159 | Common:2; Rare:32 | ||||
| chr11:65662872-65663321 | Common:4; Rare:113 | ||||
| chr11:65663466-65663475 | Rare:1 | ||||
| chr11:65711906-65712018 | Rare:39 | ||||
| chr11:65712224-65712270 | Rare:17 | ||||
| chr11:65720452-65720579 | Common:1; Rare:72 | ||||
| chr11:65856952-65857356 | Common:4; Rare:122 | ||||
| chr11:65860182-65860459 | Common:1; Rare:93 | ||||
| chr11:65860480-65860763 | Common:1; Rare:90 | ||||
| chr11:65867045-65867110 | Rare:21; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:65872726-65872961 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:65873550-65873800 | Common:3; Rare:79 | ||||
| chr11:65879551-65879842 | Common:5; Rare:55 |