| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31605665-31606065 | Common:2; Rare:207 | ||||
| chr20:31722216-31722723 | Common:7; Rare:434 | ||||
| chr20:31722762-31723830 | Common:14; Rare:1175 | ||||
| chr20:31723792-31724254 | Rare:219 | ||||
| chr20:31738765-31738914 | Rare:32 | ||||
| chr20:31738983-31739586 | Common:24; Rare:680 | ||||
| chr20:31879576-31880215 | Common:2; Rare:408 | ||||
| chr20:31951899-31952328 | Common:3; Rare:363 | ||||
| chr20:32109290-32109600 | Common:2; Rare:103 | ||||
| chr20:32109620-32110049 | Common:1; Rare:259 | ||||
| chr20:32109970-32110550 | Rare:220 | ||||
| chr20:32206998-32207490 | Rare:331 | ||||
| chr20:32207592-32207992 | Common:21; Rare:750 | ||||
| chr20:32277251-32277801 | Rare:409 | ||||
| chr20:32357640-32358544 | Common:31; Rare:989; Clinvar:5; Clinvar (benign):2 |