| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31475125-31475326 | Common:1; Rare:40 | ||||
| chr20:31547272-31547437 | Rare:44 | ||||
| chr20:31605680-31605806 | Common:1; Rare:64 | ||||
| chr20:31722726-31722956 | Rare:58 | ||||
| chr20:31723527-31723715 | Common:1; Rare:51 | ||||
| chr20:32207694-32207971 | Common:3; Rare:111 | ||||
| chr20:33401481-33401633 | Rare:41 | ||||
| chr20:33993672-33993978 | Common:3; Rare:100 | ||||
| chr20:34303281-34303315 | Common:1; Rare:25; Clinvar (benign):1 | ||||
| chr20:34516303-34516450 | Common:3; Rare:57 | ||||
| chr20:34558525-34558776 | Common:1; Rare:68 | ||||
| chr20:34677081-34677304 | Rare:57 | ||||
| chr20:34876315-34876670 | Common:3; Rare:97 | ||||
| chr20:34955743-34955836 | Common:1; Rare:35; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:35171910-35172114 | Rare:34 |