| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45060904-45061459 | Common:3; Rare:158 | ||||
| chr17:45105371-45105836 | Common:4; Rare:108 | ||||
| chr17:45118425-45118557 | Rare:45 | ||||
| chr17:45132542-45132642 | Rare:37 | ||||
| chr17:45148142-45148574 | Common:1; Rare:143 | ||||
| chr17:45161494-45161817 | Common:1; Rare:83 | ||||
| chr17:45316973-45317346 | Common:5; Rare:94 | ||||
| chr17:45894278-45894563 | Common:2; Rare:85; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:46045612-46045668 | Rare:10 | ||||
| chr17:46192836-46193217 | Common:4; Rare:97 | ||||
| chr17:46193377-46193605 | Common:3; Rare:60 | ||||
| chr17:46923020-46923257 | Common:3; Rare:99; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr17:47189172-47189591 | Common:1; Rare:114 | ||||
| chr17:47530985-47531216 | Rare:55 | ||||
| chr17:47531252-47531469 | Common:2; Rare:74 |