| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80036578-80036668 | Common:2; Rare:23; Clinvar (benign):2 | ||||
| chr17:80101373-80101633 | Common:4; Rare:113; Clinvar (benign):3 | ||||
| chr17:80147075-80147320 | Common:5; Rare:102 | ||||
| chr17:80220309-80220468 | Common:1; Rare:61; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415109-80415197 | Common:1; Rare:59 | ||||
| chr17:80991611-80991928 | Common:2; Rare:92 | ||||
| chr17:81239036-81239317 | Common:2; Rare:92 | ||||
| chr17:81295273-81295398 | Common:1; Rare:24 | ||||
| chr17:81552346-81552457 | Common:1; Rare:41 | ||||
| chr17:81666552-81666761 | Common:1; Rare:90 | ||||
| chr17:81683676-81684057 | Common:4; Rare:193 | ||||
| chr17:81703290-81703517 | Common:2; Rare:63; Clinvar (benign):2 | ||||
| chr17:81833242-81833371 | Rare:55 | ||||
| chr17:81871303-81871445 | Rare:47 | ||||
| chr17:81918137-81918236 | Rare:40 |