| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74466101-74466406 | Common:3; Rare:64 | ||||
| chr17:74466578-74466694 | Rare:36 | ||||
| chr17:74737133-74737275 | Rare:51 | ||||
| chr17:74748417-74748708 | Common:4; Rare:105 | ||||
| chr17:74776250-74776550 | Common:4; Rare:98 | ||||
| chr17:74958660-74959004 | Common:2; Rare:81 | ||||
| chr17:74972619-74972865 | Common:2; Rare:65 | ||||
| chr17:75012635-75012719 | Common:1; Rare:29 | ||||
| chr17:75046926-75047176 | Common:1; Rare:76 | ||||
| chr17:75109878-75109982 | Common:1; Rare:26 | ||||
| chr17:75130506-75131099 | Common:3; Rare:212 | ||||
| chr17:75131401-75131782 | Common:4; Rare:138 | ||||
| chr17:75205370-75205749 | Common:1; Rare:122 | ||||
| chr17:75261559-75261929 | Common:4; Rare:120; Clinvar (benign):2 | ||||
| chr17:75271146-75271354 | Common:2; Rare:38 |