| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6603542-6603822 | Common:4; Rare:86; Clinvar (benign):3 | ||||
| chr11:6604059-6604313 | Common:1; Rare:67; Clinvar (benign):2 | ||||
| chr11:6683261-6683652 | Common:6; Rare:148 | ||||
| chr11:7020318-7020517 | Rare:73 | ||||
| chr11:7513625-7513991 | Common:6; Rare:112 | ||||
| chr11:7577316-7577545 | Common:12; Rare:82 | ||||
| chr11:7673448-7673574 | Common:1; Rare:43 | ||||
| chr11:8593932-8594045 | Common:1; Rare:36 | ||||
| chr11:8682644-8683265 | Common:4; Rare:238 | ||||
| chr11:8717948-8718187 | Common:6; Rare:55 | ||||
| chr11:8932995-8933141 | Common:1; Rare:36 | ||||
| chr11:8964323-8964553 | Common:4; Rare:85 | ||||
| chr11:8964916-8964982 | Common:1; Rare:14 | ||||
| chr11:9265403-9265486 | Common:1; Rare:30 | ||||
| chr11:9314568-9314897 | Common:3; Rare:105 |