| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:68820733-68821090 | Rare:106 | ||||
| chr15:69160333-69160662 | Common:4; Rare:102 | ||||
| chr15:69414201-69414453 | Rare:85 | ||||
| chr15:69452688-69452919 | Common:4; Rare:104 | ||||
| chr15:70096223-70096332 | Rare:40 | ||||
| chr15:70096370-70096411 | Rare:9 | ||||
| chr15:70097375-70097559 | Common:1; Rare:57 | ||||
| chr15:70854096-70854330 | Rare:82 | ||||
| chr15:70892352-70892619 | Common:1; Rare:60 | ||||
| chr15:70892708-70892929 | Rare:64 | ||||
| chr15:72117827-72118439 | Common:5; Rare:212 | ||||
| chr15:72231123-72231355 | Common:2; Rare:78 | ||||
| chr15:72272482-72272812 | Common:1; Rare:96 | ||||
| chr15:72306305-72306751 | Common:2; Rare:59 | ||||
| chr15:72375938-72376161 | Common:3; Rare:90; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):5 |