| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79839417-79839712 | Rare:75 | ||||
| chr17:79950600-79951060 | Common:3; Rare:92 | ||||
| chr17:79951528-79951696 | Common:1; Rare:47 | ||||
| chr17:79951938-79952188 | Common:2; Rare:58 | ||||
| chr17:79993680-79994040 | Common:1; Rare:78 | ||||
| chr17:80035838-80036092 | Common:2; Rare:87 | ||||
| chr17:80036514-80036681 | Common:2; Rare:45; Clinvar (benign):2 | ||||
| chr17:80036850-80037076 | Common:1; Rare:62 | ||||
| chr17:80101415-80101610 | Common:3; Rare:89; Clinvar (benign):2 | ||||
| chr17:80102199-80102447 | Common:2; Rare:46 | ||||
| chr17:80116434-80116834 | Common:5; Rare:130 | ||||
| chr17:80146969-80147445 | Common:10; Rare:204 | ||||
| chr17:80220309-80220468 | Common:1; Rare:61; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80260300-80260920 | Common:12; Rare:106 | ||||
| chr17:80415068-80415233 | Common:1; Rare:115 |