| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46617080-46617594 | Common:5; Rare:183 | ||||
| chr11:46617850-46618160 | Common:3; Rare:111 | ||||
| chr11:46700517-46700842 | Common:2; Rare:156 | ||||
| chr11:46700919-46701106 | Common:4; Rare:100 | ||||
| chr11:46718876-46719325 | Common:1; Rare:148; Clinvar:1 | ||||
| chr11:46846204-46846415 | Common:2; Rare:120 | ||||
| chr11:46936611-46936822 | Common:4; Rare:116 | ||||
| chr11:47176797-47177198 | Common:2; Rare:294 | ||||
| chr11:47185360-47185680 | Common:2; Rare:74 | ||||
| chr11:47186374-47186544 | Rare:51 | ||||
| chr11:47214200-47214672 | Common:3; Rare:79 | ||||
| chr11:47214827-47215127 | Common:4; Rare:156; Clinvar:6; Clinvar (benign):2 | ||||
| chr11:47248430-47248710 | Common:2; Rare:124; Clinvar (benign):2 | ||||
| chr11:47248765-47248968 | Rare:148 | ||||
| chr11:47249219-47249490 | Common:2; Rare:71 |