| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18634313-18634580 | Common:2; Rare:86 | ||||
| chr11:18698533-18698758 | Common:4; Rare:57 | ||||
| chr11:19201952-19202170 | Rare:43; Clinvar (benign):5 | ||||
| chr11:20023204-20023262 | Rare:7 | ||||
| chr11:20387455-20387765 | Common:7; Rare:101 | ||||
| chr11:20669465-20669641 | Common:2; Rare:81 | ||||
| chr11:22192920-22193116 | Rare:42 | ||||
| chr11:22625476-22625618 | Rare:69; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr11:22625801-22626006 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:27362975-27363396 | Common:1; Rare:179 | ||||
| chr11:27506738-27506875 | Common:1; Rare:59 | ||||
| chr11:28108072-28108424 | Common:2; Rare:104 | ||||
| chr11:30016963-30017058 | Rare:25 | ||||
| chr11:30322928-30323183 | Common:3; Rare:75 | ||||
| chr11:30583992-30584150 | Rare:41 |