| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14643627-14643960 | Common:1; Rare:113 | ||||
| chr11:14891620-14891826 | Rare:60 | ||||
| chr11:14892149-14892399 | Rare:89 | ||||
| chr11:16738438-16738854 | Common:3; Rare:101 | ||||
| chr11:17012806-17013179 | Common:5; Rare:65 | ||||
| chr11:17013850-17013994 | Common:6; Rare:61 | ||||
| chr11:17014185-17014330 | Rare:57 | ||||
| chr11:17077583-17077731 | Common:2; Rare:69 | ||||
| chr11:17207911-17208111 | Common:2; Rare:75 | ||||
| chr11:17276465-17276816 | Common:4; Rare:102; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:17544303-17544497 | Common:3; Rare:50; Clinvar:2 | ||||
| chr11:18012896-18013246 | Common:6; Rare:117 | ||||
| chr11:18106045-18106308 | Common:2; Rare:75 | ||||
| chr11:18322108-18322330 | Common:4; Rare:86; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322476-18322616 | Common:2; Rare:59 |