| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:64144518-64144637 | Rare:22 | ||||
| chr15:64144694-64145150 | Common:7; Rare:240 | ||||
| chr15:64159961-64160474 | Common:5; Rare:276; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):6 | ||||
| chr15:64430380-64430744 | Common:1; Rare:86 | ||||
| chr15:64461480-64461840 | Common:4; Rare:86 | ||||
| chr15:64507613-64507742 | Rare:13 | ||||
| chr15:64532543-64532943 | Common:1; Rare:99 | ||||
| chr15:64571888-64572288 | Common:1; Rare:125 | ||||
| chr15:64574660-64575060 | Common:1; Rare:126 | ||||
| chr15:64597170-64597580 | Common:2; Rare:130 | ||||
| chr15:64600763-64601163 | Rare:111 | ||||
| chr15:64622900-64623370 | Common:2; Rare:131 | ||||
| chr15:64623608-64624434 | Common:4; Rare:155 | ||||
| chr15:64634163-64634385 | Common:2; Rare:85 | ||||
| chr15:64634737-64634931 | Rare:43 |