| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:56918402-56918832 | Common:3; Rare:149 | ||||
| chr15:58749592-58750074 | Common:4; Rare:154 | ||||
| chr15:58771039-58771325 | Common:2; Rare:111 | ||||
| chr15:58893342-58893604 | Common:3; Rare:46 | ||||
| chr15:58933516-58933775 | Common:2; Rare:114 | ||||
| chr15:59372541-59372694 | Common:1; Rare:38 | ||||
| chr15:59372815-59373038 | Common:2; Rare:70 | ||||
| chr15:59689145-59689456 | Common:7; Rare:142 | ||||
| chr15:60397914-60398158 | Common:2; Rare:57 | ||||
| chr15:60479060-60479213 | Common:2; Rare:65 | ||||
| chr15:62060364-62060513 | Rare:59 | ||||
| chr15:62165278-62165384 | Common:1; Rare:28 | ||||
| chr15:62390441-62390632 | Common:1; Rare:86 | ||||
| chr15:63042463-63042952 | Common:6; Rare:151; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63043019-63043232 | Common:1; Rare:35 |