| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58888781-58889202 | Common:2; Rare:264 | ||||
| chr20:58890893-58891445 | Common:10; Rare:372 | ||||
| chr20:58891459-58892211 | Common:13; Rare:495; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr20:58903562-58903735 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr20:58981059-58981370 | Common:5; Rare:253 | ||||
| chr20:59032269-59032633 | Common:8; Rare:280; Clinvar (benign):8 | ||||
| chr20:59042753-59043041 | Common:1; Rare:106 | ||||
| chr20:59940238-59940495 | Rare:189 | ||||
| chr20:59940630-59941130 | Common:3; Rare:113 | ||||
| chr20:62065799-62066062 | Common:4; Rare:224 | ||||
| chr20:62121756-62122536 | Common:13; Rare:362 | ||||
| chr20:62143288-62143829 | Common:13; Rare:455 | ||||
| chr20:62182891-62183098 | Common:3; Rare:158 | ||||
| chr20:62302699-62303266 | Common:4; Rare:244 | ||||
| chr20:62367233-62367840 | Common:5; Rare:287 |