| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74748316-74748704 | Common:5; Rare:138 | ||||
| chr17:74748890-74749194 | Common:3; Rare:111; Clinvar:2 | ||||
| chr17:74776061-74776154 | Rare:19 | ||||
| chr17:74776204-74776560 | Common:5; Rare:108 | ||||
| chr17:74872619-74872802 | Common:1; Rare:45 | ||||
| chr17:74872921-74873048 | Common:2; Rare:53; Clinvar (pathogenic):1 | ||||
| chr17:74873089-74873695 | Common:6; Rare:171 | ||||
| chr17:74893619-74893812 | Rare:48 | ||||
| chr17:74972117-74972229 | Rare:23 | ||||
| chr17:74972662-74972880 | Common:3; Rare:66 | ||||
| chr17:74987451-74987766 | Rare:92 | ||||
| chr17:75012363-75012795 | Common:2; Rare:106 | ||||
| chr17:75012813-75013151 | Common:3; Rare:94 | ||||
| chr17:75046192-75046541 | Common:3; Rare:73 | ||||
| chr17:75046569-75046703 | Common:4; Rare:40 |