| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:66357049-66357166 | Common:1; Rare:22 | ||||
| chr15:66386575-66387062 | Common:4; Rare:160; Clinvar:3; Clinvar (benign):6 | ||||
| chr15:66387252-66387633 | Common:7; Rare:110; Clinvar:2; Clinvar (benign):7 | ||||
| chr15:66497629-66497859 | Common:1; Rare:108 | ||||
| chr15:66497876-66498154 | Common:1; Rare:79 | ||||
| chr15:66504562-66505196 | Common:4; Rare:226 | ||||
| chr15:66505238-66505456 | Common:3; Rare:99 | ||||
| chr15:66505466-66505678 | Rare:46 | ||||
| chr15:66505741-66505862 | Common:1; Rare:21 | ||||
| chr15:67065311-67065958 | Common:2; Rare:212; Clinvar:2 | ||||
| chr15:67098554-67098734 | Common:1; Rare:39 | ||||
| chr15:67125622-67125896 | Common:3; Rare:49 | ||||
| chr15:67184440-67184725 | Common:3; Rare:62; Clinvar (benign):2 | ||||
| chr15:67254187-67254435 | Common:1; Rare:50 | ||||
| chr15:67254488-67254927 | Common:1; Rare:171 |