| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69013590-69013993 | Common:2; Rare:134 | ||||
| chr3:69052219-69052429 | Common:3; Rare:75 | ||||
| chr3:69386076-69386240 | Rare:37 | ||||
| chr3:71581927-71582183 | Common:1; Rare:63 | ||||
| chr3:72848370-72848515 | Rare:55 | ||||
| chr3:79767537-79767634 | Rare:17 | ||||
| chr3:79767940-79768068 | Rare:21 | ||||
| chr3:81761523-81761830 | Common:8; Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058906-88059308 | Common:3; Rare:154 | ||||
| chr3:88149613-88149690 | Common:1; Rare:20 | ||||
| chr3:88149856-88150063 | Common:5; Rare:83 | ||||
| chr3:93979927-93980190 | Common:3; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:94062897-94063091 | Rare:47 | ||||
| chr3:96814118-96814126 | Rare:2 | ||||
| chr3:96814406-96814626 | Rare:81 |