| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:56918285-56918821 | Common:4; Rare:196 | ||||
| chr15:58749600-58750028 | Common:4; Rare:135 | ||||
| chr15:58770975-58771328 | Common:3; Rare:138 | ||||
| chr15:58933516-58933769 | Common:2; Rare:110 | ||||
| chr15:58988038-58988184 | Common:1; Rare:45 | ||||
| chr15:59372535-59372706 | Common:1; Rare:45 | ||||
| chr15:59372751-59373048 | Common:3; Rare:103 | ||||
| chr15:60478907-60479213 | Common:3; Rare:119 | ||||
| chr15:62060349-62060537 | Rare:74 | ||||
| chr15:62165281-62165384 | Rare:28 | ||||
| chr15:63042498-63043141 | Common:5; Rare:185; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr15:63043244-63043660 | Rare:97 | ||||
| chr15:63048335-63048719 | Common:4; Rare:140; Clinvar:5; Clinvar (benign):4 | ||||
| chr15:63056731-63057161 | Common:3; Rare:96; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:63157402-63157548 | Common:2; Rare:63 |