| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:90134499-90134922 | Common:1; Rare:130 | ||||
| chr11:90222922-90223257 | Common:3; Rare:134 | ||||
| chr11:93197421-93197522 | Common:1; Rare:18 | ||||
| chr11:93197835-93198162 | Common:3; Rare:98 | ||||
| chr11:93543297-93543555 | Common:3; Rare:70 | ||||
| chr11:93661509-93661782 | Common:1; Rare:73 | ||||
| chr11:93741186-93741260 | Rare:18 | ||||
| chr11:93741304-93741723 | Common:8; Rare:161 | ||||
| chr11:93784169-93784409 | Common:3; Rare:72 | ||||
| chr11:93784832-93784933 | Common:1; Rare:27 | ||||
| chr11:94128730-94129204 | Common:4; Rare:162 | ||||
| chr11:94129382-94129495 | Rare:38 | ||||
| chr11:94401166-94401336 | Common:2; Rare:65 | ||||
| chr11:94493531-94493597 | Rare:20 | ||||
| chr11:94493748-94494072 | Common:6; Rare:93; Clinvar:1; Clinvar (benign):2 |