| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:65286850-65287023 | Rare:55 | ||||
| chr15:65530334-65530543 | Common:3; Rare:89 | ||||
| chr15:65611072-65611397 | Common:3; Rare:111 | ||||
| chr15:65792066-65792470 | Common:3; Rare:115 | ||||
| chr15:65869395-65869622 | Rare:90 | ||||
| chr15:66293464-66293631 | Common:4; Rare:54 | ||||
| chr15:66386670-66386950 | Common:2; Rare:106; Clinvar:3; Clinvar (benign):4 | ||||
| chr15:66387064-66387365 | Common:4; Rare:85; Clinvar:2; Clinvar (benign):5 | ||||
| chr15:66504789-66505179 | Common:2; Rare:148 | ||||
| chr15:66701952-66702337 | Common:2; Rare:126 | ||||
| chr15:67065389-67065671 | Common:1; Rare:101 | ||||
| chr15:67065803-67066164 | Common:3; Rare:95; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr15:67254565-67254885 | Common:1; Rare:127 | ||||
| chr15:67520933-67521251 | Common:5; Rare:117 | ||||
| chr15:67521585-67521673 | Rare:27 |