| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:58749482-58749584 | Rare:36 | ||||
| chr15:58749629-58749895 | Common:3; Rare:85 | ||||
| chr15:58770994-58771327 | Common:3; Rare:129 | ||||
| chr15:58933474-58933849 | Common:3; Rare:166 | ||||
| chr15:59372528-59372703 | Common:1; Rare:46 | ||||
| chr15:59372799-59373047 | Common:2; Rare:82 | ||||
| chr15:59689119-59689575 | Common:9; Rare:200 | ||||
| chr15:60479012-60479201 | Common:2; Rare:86 | ||||
| chr15:61856539-61856660 | Common:2; Rare:15 | ||||
| chr15:62060275-62060538 | Rare:97 | ||||
| chr15:62390430-62390603 | Rare:93 | ||||
| chr15:62740244-62740426 | Common:1; Rare:34 | ||||
| chr15:63042582-63043243 | Common:2; Rare:178; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr15:63048284-63048707 | Common:4; Rare:156; Clinvar:5; Clinvar (benign):4 | ||||
| chr15:63049268-63049431 | Common:1; Rare:40 |