| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:11466733-11466860 | Common:1; Rare:48 | ||||
| chr8:11676810-11677041 | Common:1; Rare:64 | ||||
| chr8:11692514-11692644 | Common:1; Rare:36 | ||||
| chr8:11704089-11704279 | Common:1; Rare:55 | ||||
| chr8:11769558-11769781 | Common:5; Rare:97 | ||||
| chr8:11795259-11795623 | Common:9; Rare:175 | ||||
| chr8:11795891-11796010 | Rare:63 | ||||
| chr8:11802396-11802817 | Common:7; Rare:243 | ||||
| chr8:11808724-11808877 | Common:7; Rare:99 | ||||
| chr8:11845727-11846016 | Common:3; Rare:171 | ||||
| chr8:11849051-11849273 | Common:2; Rare:109 | ||||
| chr8:11868006-11868327 | Rare:152 | ||||
| chr8:13133233-13133642 | Common:13; Rare:115 | ||||
| chr8:15540200-15540469 | Common:4; Rare:112; Clinvar:11; Clinvar (benign):1 | ||||
| chr8:17027090-17027261 | Common:3; Rare:79 |