| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:13784892-13785065 | Common:2; Rare:71; Clinvar (benign):2 | ||||
| chr20:16573321-16573540 | Common:1; Rare:59 | ||||
| chr20:17968472-17968605 | Common:4; Rare:59 | ||||
| chr20:17968788-17969122 | Common:3; Rare:118 | ||||
| chr20:18567295-18567467 | Common:3; Rare:63 | ||||
| chr20:20017202-20017402 | Rare:68 | ||||
| chr20:21303264-21303386 | Rare:53 | ||||
| chr20:24992698-24992827 | Common:3; Rare:59 | ||||
| chr20:25247940-25248125 | Common:1; Rare:73 | ||||
| chr20:25696831-25697085 | Common:3; Rare:66 | ||||
| chr20:31739098-31739369 | Common:1; Rare:71 | ||||
| chr20:32207712-32207944 | Common:3; Rare:91 | ||||
| chr20:33401491-33401582 | Rare:24 | ||||
| chr20:34112168-34112491 | Common:1; Rare:109 | ||||
| chr20:34516278-34516451 | Common:3; Rare:69 |