| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18341326-18341562 | Rare:71 | ||||
| chr11:18394263-18394644 | Common:2; Rare:135; Clinvar (benign):1 | ||||
| chr11:18526790-18526991 | Common:1; Rare:89 | ||||
| chr11:18588624-18588910 | Common:2; Rare:103 | ||||
| chr11:18589045-18589235 | Rare:41 | ||||
| chr11:18634201-18634497 | Common:2; Rare:109 | ||||
| chr11:20364047-20364418 | Common:5; Rare:117 | ||||
| chr11:20387420-20387777 | Common:7; Rare:116 | ||||
| chr11:22625481-22625618 | Rare:66; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr11:22625754-22626002 | Common:2; Rare:94; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:27506717-27506862 | Common:1; Rare:67 | ||||
| chr11:28108068-28108414 | Common:2; Rare:102 | ||||
| chr11:30322971-30323183 | Common:2; Rare:61 | ||||
| chr11:31369723-31369911 | Rare:56 | ||||
| chr11:31509557-31509827 | Common:1; Rare:96 |