| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34105381-34105810 | Common:10; Rare:320 | ||||
| chr11:34357884-34358347 | Common:8; Rare:348 | ||||
| chr11:34438704-34439045 | Common:4; Rare:197; Clinvar (benign):2 | ||||
| chr11:34513280-34513640 | Common:3; Rare:67 | ||||
| chr11:34513699-34513836 | Rare:28 | ||||
| chr11:34620800-34621150 | Common:3; Rare:78 | ||||
| chr11:34632020-34632530 | Common:2; Rare:88 | ||||
| chr11:34915691-34916091 | Common:8; Rare:117 | ||||
| chr11:34916242-34916756 | Common:31; Rare:467; Clinvar:18; Clinvar (benign):34; Clinvar (pathogenic):2 | ||||
| chr11:35138992-35139256 | Common:1; Rare:103 | ||||
| chr11:35139616-35139900 | Common:5; Rare:92 | ||||
| chr11:35287102-35287211 | Rare:15 | ||||
| chr11:35419340-35419750 | Common:10; Rare:194 | ||||
| chr11:35618226-35618491 | Common:3; Rare:82 | ||||
| chr11:35619020-35619680 | Common:2; Rare:388 |