| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:37096529-37097719 | Common:4; Rare:379 | ||||
| chr15:37097718-37098429 | Common:7; Rare:259; Clinvar (benign):2 | ||||
| chr15:37098654-37098812 | Rare:34 | ||||
| chr15:37100378-37100689 | Common:1; Rare:85 | ||||
| chr15:37101232-37101459 | Common:24; Rare:81 | ||||
| chr15:37101640-37101970 | Common:2; Rare:101 | ||||
| chr15:38251783-38252018 | Common:1; Rare:78 | ||||
| chr15:38252174-38252369 | Common:1; Rare:90 | ||||
| chr15:38252790-38253440 | Common:2; Rare:271; Clinvar:12; Clinvar (benign):11 | ||||
| chr15:38454037-38454212 | Rare:64 | ||||
| chr15:38454352-38454752 | Common:2; Rare:137 | ||||
| chr15:38564632-38565032 | Common:3; Rare:163 | ||||
| chr15:39580873-39581110 | Common:1; Rare:65 | ||||
| chr15:39782763-39783044 | Common:1; Rare:84 | ||||
| chr15:39920912-39921088 | Common:2; Rare:62 |