| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79009744-79009924 | Common:8; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:79022641-79022895 | Common:2; Rare:43 | ||||
| chr17:79025339-79025714 | Common:6; Rare:69 | ||||
| chr17:80035843-80036031 | Common:1; Rare:66 | ||||
| chr17:80147081-80147331 | Common:5; Rare:101 | ||||
| chr17:80219542-80219834 | Common:1; Rare:54 | ||||
| chr17:80220309-80220469 | Common:1; Rare:62; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80372726-80373025 | Common:1; Rare:79 | ||||
| chr17:80384808-80385080 | Rare:59 | ||||
| chr17:80385288-80385589 | Common:1; Rare:87 | ||||
| chr17:80415115-80415200 | Common:1; Rare:59 | ||||
| chr17:80415385-80415492 | Common:4; Rare:40 | ||||
| chr17:81239048-81239321 | Common:2; Rare:90 | ||||
| chr17:81294877-81295025 | Common:2; Rare:38 | ||||
| chr17:81295266-81295433 | Common:2; Rare:39 |