| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40104237-40105506 | Common:17; Rare:535 | ||||
| chr15:40115909-40116025 | Common:1; Rare:31 | ||||
| chr15:40155220-40155570 | Common:2; Rare:66 | ||||
| chr15:40245170-40245590 | Rare:69 | ||||
| chr15:40323352-40323758 | Common:9; Rare:233 | ||||
| chr15:40342950-40343280 | Common:3; Rare:59 | ||||
| chr15:40436130-40436440 | Common:4; Rare:144 | ||||
| chr15:40471756-40472045 | Rare:92; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr15:40511550-40512200 | Common:6; Rare:222 | ||||
| chr15:40582820-40583170 | Rare:76 | ||||
| chr15:40756960-40757400 | Common:7; Rare:71 | ||||
| chr15:40785810-40786090 | Common:1; Rare:42 | ||||
| chr15:40787440-40787761 | Rare:91 | ||||
| chr15:40815314-40815604 | Common:1; Rare:51 | ||||
| chr15:40823530-40823930 | Common:2; Rare:172 |