| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:38252410-38252590 | Rare:145 | ||||
| chr15:39782650-39783050 | Common:3; Rare:175 | ||||
| chr15:39920876-39921088 | Common:6; Rare:145 | ||||
| chr15:39933973-39934235 | Common:8; Rare:166 | ||||
| chr15:39953760-39954130 | Rare:136; Clinvar (pathogenic):2 | ||||
| chr15:40039088-40039354 | Common:2; Rare:204 | ||||
| chr15:40160886-40161233 | Common:8; Rare:129; Clinvar (benign):2 | ||||
| chr15:40307901-40308067 | Common:2; Rare:80 | ||||
| chr15:40358020-40358370 | Common:17; Rare:263 | ||||
| chr15:40382812-40383037 | Common:2; Rare:200 | ||||
| chr15:40405591-40405839 | Common:4; Rare:136; Clinvar (benign):7; Clinvar (pathogenic):6 | ||||
| chr15:40440683-40441213 | Rare:225 | ||||
| chr15:40470860-40471056 | Rare:125 | ||||
| chr15:40564960-40565257 | Common:6; Rare:92 | ||||
| chr15:40569201-40569374 | Common:3; Rare:46 |