| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18588667-18588929 | Common:3; Rare:86 | ||||
| chr11:18634332-18634580 | Common:2; Rare:79 | ||||
| chr11:18698520-18698748 | Common:3; Rare:51 | ||||
| chr11:20669465-20669599 | Common:2; Rare:62 | ||||
| chr11:22625507-22625609 | Rare:50; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626035 | Common:3; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:26721961-26722258 | Common:3; Rare:53 | ||||
| chr11:27363068-27363316 | Rare:111 | ||||
| chr11:27506721-27506877 | Common:1; Rare:72 | ||||
| chr11:28108115-28108424 | Common:1; Rare:95 | ||||
| chr11:30016968-30017103 | Rare:40 | ||||
| chr11:30322983-30323199 | Common:2; Rare:62 | ||||
| chr11:30584090-30584220 | Rare:26 | ||||
| chr11:31369724-31369887 | Rare:50 | ||||
| chr11:31509536-31509942 | Common:2; Rare:149 |