| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:121291663-121291962 | Common:1; Rare:58 | ||||
| chr11:121292402-121292936 | Rare:304; Clinvar:9 | ||||
| chr11:121452179-121452429 | Common:2; Rare:122 | ||||
| chr11:121452548-121453190 | Common:5; Rare:179 | ||||
| chr11:122882440-122882956 | Common:6; Rare:229 | ||||
| chr11:123062027-123062443 | Common:10; Rare:383 | ||||
| chr11:123062398-123062710 | Common:8; Rare:254 | ||||
| chr11:123062628-123062784 | Rare:59 | ||||
| chr11:123062847-123063129 | Common:4; Rare:163 | ||||
| chr11:123083570-123083910 | Common:2; Rare:117; Clinvar (pathogenic):2 | ||||
| chr11:123194859-123195026 | Common:3; Rare:64 | ||||
| chr11:123454003-123454490 | Common:4; Rare:217 | ||||
| chr11:123741555-123741827 | Common:3; Rare:112 | ||||
| chr11:124622709-124622966 | Common:13; Rare:193 | ||||
| chr11:124673629-124674055 | Common:14; Rare:273 |