| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:56918277-56918798 | Common:4; Rare:189 | ||||
| chr15:58749680-58750063 | Common:4; Rare:125 | ||||
| chr15:58770981-58771323 | Common:3; Rare:136 | ||||
| chr15:58887489-58887786 | Rare:58 | ||||
| chr15:58933457-58933775 | Common:2; Rare:132 | ||||
| chr15:59372545-59372703 | Common:1; Rare:40 | ||||
| chr15:59372819-59373047 | Common:2; Rare:72 | ||||
| chr15:59689271-59689455 | Common:7; Rare:104 | ||||
| chr15:60479075-60479240 | Common:2; Rare:75 | ||||
| chr15:60592471-60592733 | Common:1; Rare:69 | ||||
| chr15:62165255-62165428 | Common:1; Rare:45 | ||||
| chr15:63042378-63042896 | Common:8; Rare:163; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63048335-63048719 | Common:4; Rare:140; Clinvar:5; Clinvar (benign):4 | ||||
| chr15:63189256-63189619 | Common:3; Rare:116 | ||||
| chr15:63277295-63277617 | Common:4; Rare:65 |