| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57514833-57515025 | Common:1; Rare:39 | ||||
| chr11:57712004-57712618 | Common:10; Rare:204 | ||||
| chr11:57761703-57761931 | Rare:43 | ||||
| chr11:58578081-58578190 | Rare:30 | ||||
| chr11:58578860-58579213 | Common:5; Rare:101 | ||||
| chr11:58905256-58905433 | Common:1; Rare:43 | ||||
| chr11:59107031-59107204 | Common:2; Rare:45 | ||||
| chr11:59142681-59142972 | Common:1; Rare:54 | ||||
| chr11:59668950-59669328 | Rare:135 | ||||
| chr11:60906399-60906651 | Rare:71 | ||||
| chr11:61311809-61312026 | Rare:68 | ||||
| chr11:61333010-61333275 | Common:1; Rare:96 | ||||
| chr11:61361835-61362038 | Common:1; Rare:49 | ||||
| chr11:61362234-61362436 | Common:2; Rare:55; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61429900-61430169 | Common:1; Rare:117; Clinvar:3; Clinvar (benign):5 |