| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39580813-39581092 | Common:1; Rare:78 | ||||
| chr15:39587950-39588170 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:39588812-39589100 | Rare:93 | ||||
| chr15:39591188-39591598 | Common:1; Rare:107 | ||||
| chr15:39593203-39593643 | Common:2; Rare:90 | ||||
| chr15:39782794-39782877 | Rare:22 | ||||
| chr15:40038864-40039350 | Common:1; Rare:172 | ||||
| chr15:40340307-40340379 | Rare:7 | ||||
| chr15:40695058-40695160 | Rare:29 | ||||
| chr15:40770199-40770438 | Rare:35 | ||||
| chr15:40776828-40777035 | Rare:35 | ||||
| chr15:40807058-40807119 | Rare:15 | ||||
| chr15:40807430-40807761 | Common:4; Rare:109 | ||||
| chr15:40844270-40844290 | Rare:1 | ||||
| chr15:40844303-40844442 | Rare:41 |