| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18106000-18106217 | Common:3; Rare:91 | ||||
| chr11:18322129-18322312 | Common:3; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322508-18322631 | Common:2; Rare:56 | ||||
| chr11:18394409-18394619 | Common:1; Rare:85; Clinvar (benign):1 | ||||
| chr11:18396028-18396410 | Common:2; Rare:126 | ||||
| chr11:18526815-18527040 | Common:2; Rare:108 | ||||
| chr11:18588667-18588941 | Common:4; Rare:86 | ||||
| chr11:18634304-18634566 | Common:3; Rare:85 | ||||
| chr11:18698505-18698747 | Common:3; Rare:54 | ||||
| chr11:18791546-18791890 | Common:1; Rare:112 | ||||
| chr11:20363659-20363735 | Common:1; Rare:17 | ||||
| chr11:20387434-20387747 | Common:7; Rare:104 | ||||
| chr11:20599260-20599524 | Common:4; Rare:57; Clinvar (benign):5 | ||||
| chr11:20669489-20669632 | Common:1; Rare:65 | ||||
| chr11:22338190-22338393 | Common:1; Rare:47 |