| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:80059809-80060031 | Common:1; Rare:161 | ||||
| chr15:80059986-80060733 | Common:11; Rare:476 | ||||
| chr15:80072301-80072701 | Common:2; Rare:156 | ||||
| chr15:80152360-80153593 | Common:61; Rare:633; Clinvar:20; Clinvar (benign):19; Clinvar (pathogenic):8 | ||||
| chr15:80155159-80156332 | Common:21; Rare:509 | ||||
| chr15:80694960-80695551 | Common:15; Rare:528 | ||||
| chr15:80988808-80989377 | Common:9; Rare:209 | ||||
| chr15:80989726-80990143 | Common:35; Rare:860 | ||||
| chr15:81000344-81001201 | Common:26; Rare:1433 | ||||
| chr15:81001143-81001543 | Common:2; Rare:135 | ||||
| chr15:81098724-81099525 | Common:18; Rare:547 | ||||
| chr15:81324054-81324516 | Common:29; Rare:666 | ||||
| chr15:82045300-82045964 | Common:8; Rare:436 | ||||
| chr15:82045960-82046592 | Common:20; Rare:902 | ||||
| chr15:82046584-82047312 | Common:6; Rare:270 |