| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18698685-18698772 | Common:2; Rare:27 | ||||
| chr11:19777541-19777828 | Common:2; Rare:71 | ||||
| chr11:20387463-20387758 | Common:5; Rare:99 | ||||
| chr11:22625499-22625611 | Rare:55; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:26994040-26994168 | Common:1; Rare:20 | ||||
| chr11:27363058-27363316 | Rare:115 | ||||
| chr11:27472762-27473032 | Common:3; Rare:58 | ||||
| chr11:27506727-27506868 | Common:1; Rare:66 | ||||
| chr11:28108134-28108421 | Common:1; Rare:86 | ||||
| chr11:30016974-30017086 | Rare:33 | ||||
| chr11:30322920-30323180 | Common:3; Rare:75 | ||||
| chr11:31369713-31369882 | Rare:52 | ||||
| chr11:31509575-31509804 | Common:1; Rare:75 | ||||
| chr11:32430727-32430970 | Common:3; Rare:50 |