| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111378715-111378898 | Common:2; Rare:35 | ||||
| chr11:111379113-111379245 | Rare:43 | ||||
| chr11:111379250-111379318 | Rare:7 | ||||
| chr11:111379352-111379583 | Common:3; Rare:48 | ||||
| chr11:111601991-111602110 | Rare:23 | ||||
| chr11:111602240-111602485 | Common:1; Rare:83 | ||||
| chr11:111765959-111765994 | Rare:10 | ||||
| chr11:111766105-111766152 | Common:2; Rare:17 | ||||
| chr11:111766308-111766469 | Common:1; Rare:103 | ||||
| chr11:111870643-111870849 | Common:2; Rare:39 | ||||
| chr11:111871143-111871403 | Common:2; Rare:76; Clinvar:1 | ||||
| chr11:111871450-111871677 | Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:111878867-111878959 | Common:2; Rare:30 | ||||
| chr11:111879000-111879549 | Common:2; Rare:195 | ||||
| chr11:111926750-111926950 | Common:4; Rare:44 |