| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75855295-75855682 | Common:1; Rare:102 | ||||
| chr17:75904879-75904982 | Common:1; Rare:40 | ||||
| chr17:75979069-75979283 | Rare:59; Clinvar:4 | ||||
| chr17:75979394-75979611 | Rare:65 | ||||
| chr17:76072503-76072664 | Rare:46 | ||||
| chr17:76103695-76103886 | Common:6; Rare:66 | ||||
| chr17:76353608-76353677 | Rare:28 | ||||
| chr17:76353855-76353985 | Rare:47 | ||||
| chr17:76501364-76501518 | Rare:53; Clinvar (benign):3 | ||||
| chr17:76540918-76541087 | Common:1; Rare:40 | ||||
| chr17:76726491-76726858 | Common:4; Rare:125 | ||||
| chr17:76737299-76737537 | Common:3; Rare:101 | ||||
| chr17:76737883-76738084 | Common:3; Rare:58 | ||||
| chr17:77140587-77141045 | Common:5; Rare:162 | ||||
| chr17:77451259-77451526 | Common:1; Rare:65 |