| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17014398-17014716 | Common:6; Rare:117 | ||||
| chr11:17077608-17077881 | Common:2; Rare:115 | ||||
| chr11:17207905-17208126 | Common:2; Rare:88 | ||||
| chr11:17276541-17276828 | Common:5; Rare:82; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:18012911-18013261 | Common:6; Rare:116 | ||||
| chr11:18322089-18322317 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322521-18322624 | Common:1; Rare:47 | ||||
| chr11:18394422-18394632 | Common:1; Rare:82; Clinvar (benign):1 | ||||
| chr11:18396170-18396436 | Rare:96 | ||||
| chr11:18526841-18527025 | Common:1; Rare:94 | ||||
| chr11:18588672-18588815 | Rare:50 | ||||
| chr11:18634326-18634588 | Common:2; Rare:84 | ||||
| chr11:18791768-18792018 | Common:1; Rare:89 | ||||
| chr11:19777535-19777832 | Common:2; Rare:78 | ||||
| chr11:20363650-20363777 | Common:2; Rare:26 |