| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:65610911-65611531 | Common:13; Rare:451 | ||||
| chr15:65611490-65611820 | Common:3; Rare:134 | ||||
| chr15:65792034-65792599 | Common:11; Rare:399 | ||||
| chr15:65869200-65869677 | Common:2; Rare:264 | ||||
| chr15:65869790-65870533 | Common:12; Rare:375 | ||||
| chr15:66293000-66293370 | Rare:100 | ||||
| chr15:66293420-66293641 | Common:12; Rare:171 | ||||
| chr15:66293640-66294097 | Common:4; Rare:224 | ||||
| chr15:66356525-66356863 | Common:3; Rare:241 | ||||
| chr15:66386584-66387078 | Common:8; Rare:417; Clinvar:9; Clinvar (benign):14 | ||||
| chr15:66497625-66497967 | Common:2; Rare:229 | ||||
| chr15:66504679-66505448 | Common:14; Rare:758 | ||||
| chr15:66701958-66702890 | Common:10; Rare:579 | ||||
| chr15:66702899-66703584 | Common:9; Rare:527; Clinvar:32; Clinvar (benign):15; Clinvar (pathogenic):3 | ||||
| chr15:66703680-66704156 | Common:5; Rare:364; Clinvar:6; Clinvar (benign):14; Clinvar (pathogenic):6 |