| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:37101711-37101923 | Common:1; Rare:70 | ||||
| chr15:38251789-38252425 | Common:3; Rare:238 | ||||
| chr15:38252440-38252646 | Common:1; Rare:85 | ||||
| chr15:38252739-38252845 | Rare:34 | ||||
| chr15:38253604-38253818 | Common:2; Rare:55 | ||||
| chr15:38454033-38454235 | Rare:77 | ||||
| chr15:38454358-38454406 | Rare:9 | ||||
| chr15:38454511-38454627 | Rare:32 | ||||
| chr15:39580813-39581084 | Common:1; Rare:76 | ||||
| chr15:39782743-39782998 | Common:1; Rare:78 | ||||
| chr15:39919967-39920234 | Common:1; Rare:56 | ||||
| chr15:39920838-39921178 | Common:4; Rare:114 | ||||
| chr15:39933906-39934224 | Common:4; Rare:107 | ||||
| chr15:39976710-39976876 | Common:2; Rare:62; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:40038639-40038782 | Common:1; Rare:29 |