| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1309545-1309842 | Common:2; Rare:123 | ||||
| chr11:3057360-3057550 | Rare:68 | ||||
| chr11:3797505-3797824 | Rare:110 | ||||
| chr11:4393666-4393787 | Rare:27 | ||||
| chr11:5624897-5625033 | Rare:20 | ||||
| chr11:6234618-6234864 | Common:2; Rare:76 | ||||
| chr11:6319741-6320004 | Rare:72 | ||||
| chr11:6390342-6390598 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:6419055-6419190 | Common:2; Rare:32 | ||||
| chr11:6481285-6481529 | Common:4; Rare:99 | ||||
| chr11:6603577-6603860 | Common:2; Rare:84; Clinvar (benign):3 | ||||
| chr11:6683271-6683635 | Common:6; Rare:139 | ||||
| chr11:7513638-7513790 | Common:1; Rare:47 | ||||
| chr11:8682641-8682799 | Common:2; Rare:67 | ||||
| chr11:8910861-8911142 | Common:4; Rare:67 |