| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18394394-18394612 | Common:1; Rare:87; Clinvar (benign):1 | ||||
| chr11:18396084-18396390 | Common:1; Rare:112 | ||||
| chr11:18526851-18527004 | Common:1; Rare:74 | ||||
| chr11:18588672-18588860 | Common:2; Rare:63 | ||||
| chr11:18634326-18634594 | Common:2; Rare:88 | ||||
| chr11:18698665-18698747 | Common:1; Rare:16 | ||||
| chr11:18791546-18791651 | Common:1; Rare:26 | ||||
| chr11:18791654-18791857 | Rare:74 | ||||
| chr11:20387379-20387647 | Common:8; Rare:88 | ||||
| chr11:20669442-20669658 | Common:3; Rare:93 | ||||
| chr11:22338223-22338410 | Common:1; Rare:38 | ||||
| chr11:22625808-22625947 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:24496364-24496675 | Common:2; Rare:43 | ||||
| chr11:24496728-24497231 | Common:4; Rare:135 | ||||
| chr11:27506729-27506868 | Common:1; Rare:65 |