| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10433902-10434075 | Common:1; Rare:41 | ||||
| chr20:10434130-10434284 | Common:2; Rare:59; Clinvar (benign):1 | ||||
| chr20:10434404-10434696 | Common:2; Rare:154 | ||||
| chr20:10435014-10435378 | Rare:185 | ||||
| chr20:10673604-10673890 | Rare:88; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:10673945-10674151 | Common:4; Rare:148; Clinvar:6; Clinvar (benign):6 | ||||
| chr20:11891211-11891740 | Common:2; Rare:244 | ||||
| chr20:13221056-13221312 | Common:5; Rare:77 | ||||
| chr20:13221515-13221915 | Common:10; Rare:199 | ||||
| chr20:13638898-13639048 | Common:1; Rare:43 | ||||
| chr20:13784840-13785098 | Common:6; Rare:226; Clinvar:2; Clinvar (benign):6 | ||||
| chr20:13785225-13785493 | Common:4; Rare:156; Clinvar:2; Clinvar (benign):6 | ||||
| chr20:15985623-15986253 | Common:11; Rare:259 | ||||
| chr20:16573264-16573601 | Common:4; Rare:204 | ||||
| chr20:16729846-16730089 | Common:1; Rare:138 |