| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80035843-80035988 | Common:1; Rare:53 | ||||
| chr17:80220309-80220483 | Common:1; Rare:64; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415022-80415197 | Common:2; Rare:109 | ||||
| chr17:80415387-80415492 | Common:4; Rare:40 | ||||
| chr17:81239029-81239315 | Common:2; Rare:95 | ||||
| chr17:81395184-81395475 | Common:1; Rare:75 | ||||
| chr17:81512118-81512376 | Common:1; Rare:131; Clinvar:3; Clinvar (benign):15 | ||||
| chr17:81636916-81637220 | Common:2; Rare:123 | ||||
| chr17:81666565-81666763 | Common:1; Rare:86 | ||||
| chr17:81683676-81684052 | Common:4; Rare:191 | ||||
| chr17:81703279-81703504 | Common:2; Rare:65; Clinvar (benign):2 | ||||
| chr17:81833248-81833399 | Rare:68 | ||||
| chr17:81871305-81871436 | Rare:44 | ||||
| chr17:81891576-81891798 | Common:3; Rare:113 | ||||
| chr17:81937180-81937415 | Rare:81 |