| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:29566964-29567285 | Rare:82 | ||||
| chr17:29567442-29567569 | Rare:23 | ||||
| chr17:29568505-29568740 | Common:3; Rare:76 | ||||
| chr17:29761273-29761568 | Common:4; Rare:110 | ||||
| chr17:30235695-30235940 | Common:2; Rare:55; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:30378781-30378980 | Common:1; Rare:76 | ||||
| chr17:30824600-30824865 | Common:3; Rare:107 | ||||
| chr17:30906205-30906354 | Common:1; Rare:42 | ||||
| chr17:31273627-31273656 | Rare:2 | ||||
| chr17:31321570-31321669 | Rare:15 | ||||
| chr17:31936915-31937049 | Rare:39 | ||||
| chr17:32142349-32142673 | Common:8; Rare:134 | ||||
| chr17:32350002-32350252 | Rare:124 | ||||
| chr17:32444426-32444561 | Rare:57 | ||||
| chr17:32445095-32445302 | Common:1; Rare:28 |