| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18634761-18634904 | Common:1; Rare:40 | ||||
| chr11:18698526-18698782 | Common:4; Rare:66 | ||||
| chr11:20363657-20363748 | Common:1; Rare:19 | ||||
| chr11:20387496-20387778 | Common:4; Rare:87 | ||||
| chr11:22625522-22625609 | Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:26994079-26994188 | Common:1; Rare:20 | ||||
| chr11:27363113-27363378 | Rare:116 | ||||
| chr11:27472742-27472866 | Common:1; Rare:33 | ||||
| chr11:27506729-27506868 | Common:1; Rare:65 | ||||
| chr11:28108120-28108414 | Common:1; Rare:89 | ||||
| chr11:30016907-30017111 | Rare:52 | ||||
| chr11:30322944-30323191 | Common:2; Rare:70 | ||||
| chr11:31369728-31369912 | Rare:55 | ||||
| chr11:31509575-31509784 | Common:1; Rare:65 |