| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25696814-25697051 | Common:3; Rare:68 | ||||
| chr20:31547312-31547487 | Rare:46 | ||||
| chr20:31722496-31722679 | Rare:39 | ||||
| chr20:31722826-31722886 | Rare:13 | ||||
| chr20:31723491-31723690 | Common:1; Rare:62 | ||||
| chr20:31739098-31739488 | Common:1; Rare:95 | ||||
| chr20:32109513-32109749 | Common:1; Rare:65 | ||||
| chr20:32207653-32208009 | Common:3; Rare:131 | ||||
| chr20:32762648-32762699 | Rare:18 | ||||
| chr20:33401476-33401582 | Rare:31 | ||||
| chr20:33993784-33994122 | Common:1; Rare:121 | ||||
| chr20:34112094-34112525 | Common:1; Rare:143 | ||||
| chr20:34303242-34303492 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:34516275-34516443 | Common:3; Rare:63 | ||||
| chr20:34677063-34677305 | Rare:66 |