| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39580808-39581182 | Common:2; Rare:106 | ||||
| chr15:39587805-39588138 | Common:1; Rare:60; Clinvar:1 | ||||
| chr15:39592595-39593227 | Common:1; Rare:133; Clinvar (benign):1 | ||||
| chr15:39782794-39782899 | Rare:28 | ||||
| chr15:39920117-39920335 | Common:1; Rare:37 | ||||
| chr15:40039091-40039349 | Rare:101 | ||||
| chr15:40252269-40252674 | Common:4; Rare:150 | ||||
| chr15:40307823-40308041 | Common:1; Rare:50 | ||||
| chr15:40405620-40405863 | Common:2; Rare:76; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr15:40569201-40569346 | Common:3; Rare:29 | ||||
| chr15:40694648-40694757 | Rare:32 | ||||
| chr15:40695075-40695168 | Rare:25 | ||||
| chr15:40755145-40755384 | Common:2; Rare:71 | ||||
| chr15:40763794-40764125 | Common:3; Rare:79 | ||||
| chr15:40770199-40770317 | Rare:20 |