| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18526841-18527001 | Common:1; Rare:77 | ||||
| chr11:18588667-18588860 | Common:2; Rare:66 | ||||
| chr11:18634336-18634580 | Common:2; Rare:78 | ||||
| chr11:18791539-18791845 | Common:1; Rare:103 | ||||
| chr11:18791848-18791860 | Rare:3 | ||||
| chr11:20669465-20669632 | Common:2; Rare:79 | ||||
| chr11:22338224-22338423 | Common:1; Rare:39 | ||||
| chr11:22625817-22626002 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:24496380-24496639 | Common:2; Rare:37 | ||||
| chr11:24496731-24496890 | Rare:44 | ||||
| chr11:24496892-24497224 | Common:4; Rare:86 | ||||
| chr11:27506721-27506864 | Common:1; Rare:66 | ||||
| chr11:28108130-28108410 | Common:1; Rare:82 | ||||
| chr11:30322928-30323154 | Common:2; Rare:67 | ||||
| chr11:30584045-30584150 | Rare:28 |