| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14891627-14891785 | Rare:47 | ||||
| chr11:14892190-14892384 | Rare:62 | ||||
| chr11:16738456-16738687 | Common:2; Rare:45 | ||||
| chr11:17014255-17014327 | Rare:26 | ||||
| chr11:17014399-17014526 | Common:1; Rare:68 | ||||
| chr11:17207910-17208111 | Common:2; Rare:76 | ||||
| chr11:17276475-17276827 | Common:5; Rare:102; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:18106050-18106308 | Common:2; Rare:71 | ||||
| chr11:18322130-18322352 | Common:6; Rare:82; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322467-18322645 | Common:2; Rare:73 | ||||
| chr11:18394427-18394630 | Common:1; Rare:80; Clinvar (benign):1 | ||||
| chr11:18526821-18527028 | Common:2; Rare:99 | ||||
| chr11:18588667-18588804 | Rare:49 | ||||
| chr11:18634326-18634572 | Common:2; Rare:77 | ||||
| chr11:18698533-18698747 | Common:3; Rare:49 |