| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40695071-40695236 | Common:2; Rare:51 | ||||
| chr15:40755209-40755456 | Common:2; Rare:84 | ||||
| chr15:40763947-40764115 | Rare:42 | ||||
| chr15:40807382-40807767 | Common:4; Rare:124 | ||||
| chr15:40894172-40894477 | Rare:88 | ||||
| chr15:40953181-40953475 | Common:1; Rare:79 | ||||
| chr15:40953631-40953637 | Rare:1 | ||||
| chr15:41115982-41116037 | Rare:20 | ||||
| chr15:41231092-41231347 | Rare:85 | ||||
| chr15:41402431-41402577 | Common:4; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:41416945-41417313 | Common:4; Rare:137 | ||||
| chr15:41544240-41544362 | Rare:49 | ||||
| chr15:41621193-41621248 | Common:1; Rare:15 | ||||
| chr15:41621414-41621552 | Common:1; Rare:32 | ||||
| chr15:41660302-41660493 | Rare:62 |