| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:16738755-16738842 | Rare:23 | ||||
| chr11:17077642-17077850 | Common:2; Rare:86 | ||||
| chr11:18322120-18322290 | Common:3; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322489-18322576 | Common:2; Rare:38 | ||||
| chr11:18526870-18527033 | Common:2; Rare:79 | ||||
| chr11:18588667-18588777 | Rare:43 | ||||
| chr11:18634293-18634590 | Common:3; Rare:101 | ||||
| chr11:27506721-27506857 | Common:1; Rare:64 | ||||
| chr11:28108120-28108392 | Rare:83 | ||||
| chr11:31509620-31509791 | Common:1; Rare:52 | ||||
| chr11:33161420-33161732 | Common:6; Rare:90 | ||||
| chr11:33257182-33257457 | Common:3; Rare:91 | ||||
| chr11:34052116-34052364 | Common:2; Rare:108 | ||||
| chr11:34105451-34105678 | Common:4; Rare:75 | ||||
| chr11:34916294-34916438 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):3 |