| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34101182-34101410 | Rare:43 | ||||
| chr15:34101810-34102192 | Common:3; Rare:213 | ||||
| chr15:34209624-34210024 | Common:4; Rare:152 | ||||
| chr15:34224824-34225131 | Rare:243 | ||||
| chr15:34318744-34318934 | Common:4; Rare:72 | ||||
| chr15:34337019-34337890 | Common:4; Rare:278 | ||||
| chr15:34337890-34338390 | Common:2; Rare:130 | ||||
| chr15:34343018-34343165 | Common:1; Rare:55; Clinvar:4; Clinvar (benign):1 | ||||
| chr15:34367094-34367457 | Common:6; Rare:312 | ||||
| chr15:34367479-34367812 | Rare:133 | ||||
| chr15:34582679-34583079 | Common:8; Rare:274 | ||||
| chr15:34583534-34583804 | Common:12; Rare:210 | ||||
| chr15:34968855-34969597 | Common:7; Rare:249 | ||||
| chr15:34969603-34969957 | Common:8; Rare:163 | ||||
| chr15:34988165-34988440 | Common:6; Rare:277 |