| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31722498-31722702 | Rare:77 | ||||
| chr20:31722784-31723001 | Rare:81 | ||||
| chr20:31723486-31723735 | Common:2; Rare:142 | ||||
| chr20:31723888-31724116 | Rare:85 | ||||
| chr20:31739048-31739559 | Common:7; Rare:193 | ||||
| chr20:31879576-31880249 | Common:6; Rare:481 | ||||
| chr20:32109396-32109774 | Common:3; Rare:144 | ||||
| chr20:32207676-32208048 | Common:7; Rare:230; Clinvar:1 | ||||
| chr20:32277519-32277706 | Rare:94 | ||||
| chr20:32357955-32358373 | Common:8; Rare:224 | ||||
| chr20:32358380-32358991 | Common:10; Rare:358; Clinvar:21; Clinvar (benign):6 | ||||
| chr20:32483444-32483769 | Common:1; Rare:93 | ||||
| chr20:32743201-32743976 | Common:5; Rare:311 | ||||
| chr20:32762084-32762444 | Common:4; Rare:203; Clinvar:1 | ||||
| chr20:32819713-32820012 | Common:6; Rare:166 |