| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:127735924-127736579 | Common:4; Rare:162 | ||||
| chr8:133297208-133297476 | Common:3; Rare:114; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:140511021-140511334 | Common:3; Rare:97 | ||||
| chr8:142669963-142670305 | Common:9; Rare:116 | ||||
| chr8:142727054-142727279 | Common:2; Rare:91 | ||||
| chr8:143018418-143018545 | Rare:35 | ||||
| chr8:143291373-143291598 | Common:4; Rare:62 | ||||
| chr8:143558267-143558390 | Common:1; Rare:48 | ||||
| chr8:143597609-143597833 | Common:2; Rare:74 | ||||
| chr8:143828990-143829180 | Common:1; Rare:70 | ||||
| chr8:143829262-143829472 | Rare:79; Clinvar:1 | ||||
| chr8:144082503-144082685 | Common:2; Rare:64 | ||||
| chr8:144096379-144096628 | Common:1; Rare:94; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr8:144103680-144103857 | Common:1; Rare:60 | ||||
| chr8:144104188-144104519 | Common:3; Rare:105 |