| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44968267-44968580 | Rare:148 | ||||
| chr17:45051350-45052151 | Common:20; Rare:350 | ||||
| chr17:45060865-45061442 | Common:6; Rare:304 | ||||
| chr17:45132384-45132678 | Common:4; Rare:190 | ||||
| chr17:45148142-45148637 | Common:2; Rare:278 | ||||
| chr17:45160395-45160880 | Common:1; Rare:180 | ||||
| chr17:45160965-45161123 | Rare:42 | ||||
| chr17:45161466-45161949 | Common:2; Rare:245 | ||||
| chr17:45221748-45221950 | Rare:55 | ||||
| chr17:45222160-45222620 | Rare:140 | ||||
| chr17:45230890-45231130 | Rare:33 | ||||
| chr17:45316935-45317353 | Common:10; Rare:195 | ||||
| chr17:45425591-45425832 | Common:1; Rare:44 | ||||
| chr17:45490681-45490921 | Common:7; Rare:76 | ||||
| chr17:45894252-45894574 | Common:5; Rare:181; Clinvar:7; Clinvar (benign):3 |