| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34053152-34053800 | Common:3; Rare:242 | ||||
| chr11:34105475-34105789 | Common:4; Rare:193 | ||||
| chr11:34357970-34358286 | Common:4; Rare:177 | ||||
| chr11:34358380-34358620 | Rare:69 | ||||
| chr11:34438757-34439047 | Common:4; Rare:180; Clinvar (benign):2 | ||||
| chr11:34513754-34514077 | Common:2; Rare:59 | ||||
| chr11:34915930-34916227 | Common:6; Rare:141; Clinvar (benign):4 | ||||
| chr11:34916248-34916740 | Common:24; Rare:351; Clinvar:12; Clinvar (benign):26; Clinvar (pathogenic):2 | ||||
| chr11:35662256-35662440 | Common:1; Rare:30 | ||||
| chr11:35662710-35662948 | Common:2; Rare:123 | ||||
| chr11:36510229-36510372 | Rare:81 | ||||
| chr11:36594314-36594561 | Common:1; Rare:48 | ||||
| chr11:43358810-43359003 | Rare:187 | ||||
| chr11:43680401-43680889 | Common:4; Rare:237 | ||||
| chr11:43880663-43880939 | Common:4; Rare:129 |