| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74203511-74203797 | Common:3; Rare:89 | ||||
| chr17:74213256-74213593 | Common:4; Rare:75 | ||||
| chr17:74748360-74748706 | Common:5; Rare:125 | ||||
| chr17:74776040-74776603 | Common:7; Rare:158 | ||||
| chr17:74872742-74872764 | Rare:4 | ||||
| chr17:74872916-74873228 | Common:4; Rare:99; Clinvar (pathogenic):1 | ||||
| chr17:74873238-74873576 | Common:5; Rare:110 | ||||
| chr17:74972685-74972874 | Common:2; Rare:50 | ||||
| chr17:74987349-74987704 | Rare:102 | ||||
| chr17:75012387-75012810 | Common:2; Rare:104 | ||||
| chr17:75012832-75013114 | Common:2; Rare:80 | ||||
| chr17:75046397-75046543 | Rare:34 | ||||
| chr17:75046588-75046633 | Rare:12 | ||||
| chr17:75046897-75047295 | Common:2; Rare:130 | ||||
| chr17:75109822-75110020 | Common:2; Rare:63 |