| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58892211-58892496 | Common:2; Rare:73 | ||||
| chr20:58892523-58892700 | Common:1; Rare:56 | ||||
| chr20:58903482-58903780 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr20:58909162-58909773 | Common:3; Rare:147; Clinvar:1; Clinvar (pathogenic):6 | ||||
| chr20:58909950-58910401 | Rare:104 | ||||
| chr20:58981098-58981364 | Common:2; Rare:118 | ||||
| chr20:58989676-58989935 | Common:1; Rare:76 | ||||
| chr20:59007144-59007411 | Common:3; Rare:73 | ||||
| chr20:59940297-59940533 | Common:1; Rare:87 | ||||
| chr20:62065785-62066054 | Common:2; Rare:116 | ||||
| chr20:62143206-62143812 | Common:8; Rare:238 | ||||
| chr20:62182942-62183052 | Rare:32 | ||||
| chr20:62302679-62303061 | Common:2; Rare:107 | ||||
| chr20:62367227-62367469 | Common:2; Rare:82 | ||||
| chr20:62386905-62387139 | Common:3; Rare:106 |