| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31723523-31723715 | Common:1; Rare:53 | ||||
| chr20:31739098-31739357 | Common:1; Rare:66 | ||||
| chr20:32207676-32207964 | Common:3; Rare:111 | ||||
| chr20:33401493-33401601 | Rare:27 | ||||
| chr20:33731987-33732010 | Rare:13 | ||||
| chr20:33993748-33994122 | Common:2; Rare:131 | ||||
| chr20:34112102-34112423 | Rare:104 | ||||
| chr20:34516279-34516451 | Common:3; Rare:69 | ||||
| chr20:34677069-34677305 | Rare:61 | ||||
| chr20:34955747-34955912 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:35171925-35172137 | Rare:44 | ||||
| chr20:35284483-35284840 | Common:3; Rare:105 | ||||
| chr20:35455059-35455214 | Common:1; Rare:56 | ||||
| chr20:35556714-35557109 | Common:2; Rare:106 | ||||
| chr20:35664867-35665012 | Common:1; Rare:38 |