| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:60351157-60351229 | Rare:23 | ||||
| chr15:60397912-60398206 | Common:2; Rare:71 | ||||
| chr15:60479065-60479270 | Common:3; Rare:89 | ||||
| chr15:62060307-62060547 | Rare:90 | ||||
| chr15:62165278-62165428 | Common:1; Rare:41 | ||||
| chr15:63041978-63042229 | Rare:46 | ||||
| chr15:63042463-63042481 | Rare:5 | ||||
| chr15:63042505-63042977 | Common:4; Rare:154; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr15:63043048-63043254 | Common:1; Rare:34 | ||||
| chr15:63048163-63048923 | Common:11; Rare:306; Clinvar:5; Clinvar (benign):4 | ||||
| chr15:63049246-63049489 | Common:1; Rare:60 | ||||
| chr15:63121712-63121863 | Rare:45 | ||||
| chr15:63156447-63156699 | Common:1; Rare:74 | ||||
| chr15:63157417-63157550 | Common:2; Rare:56 | ||||
| chr15:63277278-63277579 | Common:3; Rare:50 |