| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28717813-28717981 | Rare:35 | ||||
| chr17:28728644-28728816 | Rare:63 | ||||
| chr17:28842748-28842861 | Rare:41 | ||||
| chr17:28854969-28855051 | Rare:26 | ||||
| chr17:28897590-28897734 | Common:1; Rare:52 | ||||
| chr17:29140384-29140480 | Common:2; Rare:30 | ||||
| chr17:29180328-29180479 | Rare:32 | ||||
| chr17:29293634-29293929 | Common:2; Rare:103 | ||||
| chr17:29294046-29294297 | Common:1; Rare:109 | ||||
| chr17:29390203-29390397 | Common:1; Rare:64 | ||||
| chr17:29567759-29568078 | Common:1; Rare:66 | ||||
| chr17:29568505-29568752 | Common:3; Rare:84 | ||||
| chr17:30235695-30235976 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:30824587-30824854 | Common:3; Rare:106 | ||||
| chr17:30906194-30906327 | Common:1; Rare:46 |