| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74598334-74598536 | Common:2; Rare:169 | ||||
| chr15:74615550-74615907 | Common:7; Rare:206 | ||||
| chr15:74695948-74696162 | Rare:110 | ||||
| chr15:74725710-74726120 | Common:6; Rare:170 | ||||
| chr15:74781945-74782148 | Common:3; Rare:65 | ||||
| chr15:74843072-74843331 | Common:4; Rare:158 | ||||
| chr15:74872810-74873240 | Common:4; Rare:209 | ||||
| chr15:74873311-74873477 | Common:5; Rare:50 | ||||
| chr15:74889836-74890104 | Rare:157; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr15:74906714-74906888 | Common:2; Rare:125 | ||||
| chr15:74937916-74938276 | Common:6; Rare:227 | ||||
| chr15:74956721-74956916 | Common:1; Rare:80 | ||||
| chr15:74957075-74957249 | Common:1; Rare:103 | ||||
| chr15:74995436-74995601 | Common:4; Rare:70 | ||||
| chr15:75023419-75023691 | Common:3; Rare:69 |