| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:134831559-134831726 | Common:2; Rare:49 | ||||
| chr8:141171053-141171337 | Rare:45 | ||||
| chr8:141190069-141190344 | Common:6; Rare:96 | ||||
| chr8:141198232-141198248 | Rare:2 | ||||
| chr8:141216445-141216594 | Rare:33 | ||||
| chr8:141292726-141292876 | Rare:34 | ||||
| chr8:142681108-142681297 | Common:1; Rare:46 | ||||
| chr8:142683070-142683531 | Common:4; Rare:91 | ||||
| chr8:143281616-143281817 | Common:3; Rare:50 | ||||
| chr8:143739240-143739368 | Common:2; Rare:35 | ||||
| chr8:143792109-143792358 | Common:1; Rare:91 | ||||
| chr8:143816781-143817018 | Common:1; Rare:77 | ||||
| chr8:143927553-143928039 | Common:5; Rare:213; Clinvar:36; Clinvar (benign):12 | ||||
| chr8:143929160-143929380 | Common:2; Rare:98; Clinvar:7; Clinvar (benign):4 | ||||
| chr8:143935041-143935329 | Common:1; Rare:110; Clinvar:10; Clinvar (benign):8 |