| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:133071911-133072164 | Common:3; Rare:40 | ||||
| chr8:133072171-133072371 | Common:2; Rare:36 | ||||
| chr8:133078054-133078249 | Common:3; Rare:30 | ||||
| chr8:133144098-133144285 | Rare:34 | ||||
| chr8:133256801-133257063 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:133498726-133498733 | Rare:1 | ||||
| chr8:138062710-138062909 | Rare:38 | ||||
| chr8:140596969-140597298 | Common:2; Rare:70 | ||||
| chr8:141095537-141095688 | Common:1; Rare:33 | ||||
| chr8:141144647-141144805 | Rare:33 | ||||
| chr8:141174105-141174213 | Rare:28 | ||||
| chr8:141174911-141175192 | Rare:72 | ||||
| chr8:143042836-143043146 | Common:3; Rare:96 | ||||
| chr8:143281625-143281809 | Common:3; Rare:46 | ||||
| chr8:143816781-143817012 | Common:1; Rare:74 |