| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70702052-70702127 | Rare:13 | ||||
| chr15:70892363-70892859 | Common:1; Rare:109 | ||||
| chr15:72118167-72118432 | Common:2; Rare:87 | ||||
| chr15:72231104-72231318 | Common:1; Rare:75 | ||||
| chr15:72375926-72376137 | Common:2; Rare:84; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72474210-72474339 | Rare:43 | ||||
| chr15:72686149-72686236 | Common:2; Rare:35; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:73633177-73633573 | Common:2; Rare:152 | ||||
| chr15:73752210-73752340 | Rare:34 | ||||
| chr15:73926332-73926466 | Rare:37 | ||||
| chr15:73994587-73994801 | Rare:46 | ||||
| chr15:74202747-74203036 | Common:1; Rare:72; Clinvar:2 | ||||
| chr15:74212216-74212427 | Rare:34 | ||||
| chr15:74461107-74461314 | Rare:64 | ||||
| chr15:74540946-74541276 | Common:4; Rare:112 |