| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322033-18322358 | Common:7; Rare:113; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:18322378-18322752 | Common:2; Rare:119 | ||||
| chr11:18347216-18347302 | Common:1; Rare:16 | ||||
| chr11:18393801-18394074 | Rare:56 | ||||
| chr11:18394106-18394202 | Common:1; Rare:16 | ||||
| chr11:18394294-18394716 | Common:1; Rare:153; Clinvar (benign):1 | ||||
| chr11:18394752-18394865 | Common:1; Rare:28 | ||||
| chr11:18395817-18396067 | Common:3; Rare:55 | ||||
| chr11:18396171-18396381 | Rare:79 | ||||
| chr11:18526604-18526731 | Common:2; Rare:29 | ||||
| chr11:18526809-18527177 | Common:3; Rare:138 | ||||
| chr11:18527210-18527264 | Rare:11 | ||||
| chr11:18588627-18588902 | Common:2; Rare:100 | ||||
| chr11:18588935-18589047 | Common:1; Rare:18 | ||||
| chr11:18634255-18634531 | Common:3; Rare:102 |