| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39782794-39782877 | Rare:22 | ||||
| chr15:40038852-40039329 | Common:1; Rare:173 | ||||
| chr15:40239108-40239216 | Common:1; Rare:17 | ||||
| chr15:40358096-40358328 | Common:6; Rare:99 | ||||
| chr15:40405594-40405827 | Common:2; Rare:68; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:40569176-40569346 | Common:3; Rare:36 | ||||
| chr15:40695050-40695202 | Rare:42 | ||||
| chr15:40807050-40807143 | Rare:30 | ||||
| chr15:40807421-40807761 | Common:4; Rare:115 | ||||
| chr15:41416982-41417202 | Common:3; Rare:98 | ||||
| chr15:41660302-41660455 | Rare:40 | ||||
| chr15:41774304-41774539 | Common:1; Rare:70 | ||||
| chr15:42208248-42208404 | Rare:52 | ||||
| chr15:42273037-42273272 | Common:1; Rare:98 | ||||
| chr15:42273394-42273643 | Rare:90 |