| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40382681-40383081 | Common:7; Rare:560 | ||||
| chr15:40383232-40383632 | Common:4; Rare:144 | ||||
| chr15:40439380-40440161 | Common:9; Rare:443 | ||||
| chr15:40440070-40440709 | Common:2; Rare:226 | ||||
| chr15:40440636-40441329 | Common:1; Rare:1216 | ||||
| chr15:40470500-40471175 | Common:4; Rare:277 | ||||
| chr15:40564870-40565354 | Common:15; Rare:315 | ||||
| chr15:40569090-40569490 | Common:21; Rare:395 | ||||
| chr15:40569694-40570230 | Common:5; Rare:203 | ||||
| chr15:40593763-40594432 | Common:14; Rare:665; Clinvar (benign):1 | ||||
| chr15:40594511-40594911 | Common:4; Rare:128 | ||||
| chr15:40693978-40694378 | Common:4; Rare:82 | ||||
| chr15:40694550-40694890 | Rare:316 | ||||
| chr15:40694990-40695938 | Common:30; Rare:836; Clinvar:4 | ||||
| chr15:40737645-40738045 | Common:3; Rare:162 |