| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79183416-79183662 | Common:1; Rare:68 | ||||
| chr17:80035852-80036030 | Common:1; Rare:62 | ||||
| chr17:80146852-80147383 | Common:12; Rare:219 | ||||
| chr17:80220309-80220478 | Common:1; Rare:64; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80386055-80386336 | Common:4; Rare:62 | ||||
| chr17:80415105-80415500 | Common:5; Rare:200 | ||||
| chr17:81034822-81035153 | Common:2; Rare:126 | ||||
| chr17:81238981-81239458 | Common:4; Rare:163 | ||||
| chr17:81239962-81240242 | Rare:59 | ||||
| chr17:81247040-81247164 | Rare:40 | ||||
| chr17:81295263-81295439 | Common:2; Rare:43 | ||||
| chr17:81395179-81395462 | Common:1; Rare:71 | ||||
| chr17:81512079-81512366 | Common:2; Rare:132; Clinvar:3; Clinvar (benign):20 | ||||
| chr17:81512729-81513047 | Common:7; Rare:174; Clinvar (benign):14 | ||||
| chr17:81552337-81552479 | Common:1; Rare:58 |