| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:58749563-58750065 | Common:4; Rare:157 | ||||
| chr15:58770903-58771328 | Common:5; Rare:158 | ||||
| chr15:58933540-58933875 | Common:4; Rare:145 | ||||
| chr15:58988056-58988157 | Common:1; Rare:36 | ||||
| chr15:59372535-59372695 | Common:1; Rare:41 | ||||
| chr15:59372794-59373028 | Common:2; Rare:76 | ||||
| chr15:59689134-59689456 | Common:7; Rare:145 | ||||
| chr15:60478920-60479213 | Common:3; Rare:118 | ||||
| chr15:61229213-61229372 | Common:1; Rare:37 | ||||
| chr15:62060349-62060518 | Rare:68 | ||||
| chr15:62165278-62165384 | Common:1; Rare:28 | ||||
| chr15:62390445-62390576 | Rare:61 | ||||
| chr15:63042451-63042948 | Common:6; Rare:153; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63043049-63043141 | Common:1; Rare:11 | ||||
| chr15:63043173-63043852 | Rare:178; Clinvar:3; Clinvar (benign):8 |