| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14891637-14891797 | Rare:42 | ||||
| chr11:14892195-14892386 | Rare:58 | ||||
| chr11:16738438-16738916 | Common:3; Rare:123 | ||||
| chr11:17077618-17077877 | Common:2; Rare:110 | ||||
| chr11:17207898-17208111 | Common:2; Rare:82 | ||||
| chr11:17276447-17276816 | Common:4; Rare:107; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18012910-18013261 | Common:6; Rare:116 | ||||
| chr11:18322086-18322347 | Common:6; Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322482-18322645 | Common:2; Rare:68 | ||||
| chr11:18394405-18394623 | Common:1; Rare:89; Clinvar (benign):1 | ||||
| chr11:18526841-18526977 | Rare:66 | ||||
| chr11:18588661-18588933 | Common:3; Rare:90 | ||||
| chr11:18634307-18634596 | Common:3; Rare:97 | ||||
| chr11:18634811-18634825 | Rare:1 | ||||
| chr11:19241618-19241882 | Common:1; Rare:76 |