| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78840745-78841114 | Common:2; Rare:139 | ||||
| chr17:79009758-79009924 | Common:7; Rare:45 | ||||
| chr17:80035849-80036030 | Common:1; Rare:62 | ||||
| chr17:80036492-80036678 | Common:2; Rare:47; Clinvar (benign):2 | ||||
| chr17:80147137-80147354 | Common:4; Rare:76 | ||||
| chr17:80220289-80220468 | Common:1; Rare:72; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415099-80415492 | Common:5; Rare:199 | ||||
| chr17:81295278-81295394 | Common:1; Rare:24 | ||||
| chr17:81512830-81513177 | Common:4; Rare:143 | ||||
| chr17:81552242-81552462 | Common:1; Rare:80 | ||||
| chr17:81666558-81666764 | Common:1; Rare:90 | ||||
| chr17:81683617-81684057 | Common:5; Rare:235 | ||||
| chr17:81703286-81703504 | Common:2; Rare:61; Clinvar (benign):2 | ||||
| chr17:81833251-81833380 | Rare:57 | ||||
| chr17:81871309-81871453 | Rare:51 |