| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33753424-33753531 | Common:1; Rare:10 | ||||
| chr11:33774447-33774826 | Common:2; Rare:128 | ||||
| chr11:34051476-34051807 | Rare:119 | ||||
| chr11:34052052-34052483 | Common:5; Rare:191 | ||||
| chr11:34053459-34053518 | Rare:13 | ||||
| chr11:34105338-34105743 | Common:4; Rare:125 | ||||
| chr11:34357940-34358315 | Common:3; Rare:114 | ||||
| chr11:34438636-34439069 | Common:3; Rare:135; Clinvar (benign):1 | ||||
| chr11:34439102-34439295 | Common:3; Rare:52 | ||||
| chr11:34915747-34915784 | Common:1; Rare:4 | ||||
| chr11:34916002-34916149 | Common:1; Rare:46 | ||||
| chr11:34916249-34916732 | Common:14; Rare:195; Clinvar:8; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr11:35139006-35139241 | Common:1; Rare:52 | ||||
| chr11:35139646-35139751 | Common:2; Rare:19 | ||||
| chr11:35618154-35618471 | Common:5; Rare:88 |