| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76737317-76737721 | Common:4; Rare:143 | ||||
| chr17:76737887-76738043 | Common:3; Rare:44 | ||||
| chr17:77088585-77088783 | Common:1; Rare:53 | ||||
| chr17:77140688-77141032 | Common:1; Rare:121 | ||||
| chr17:77287789-77288023 | Rare:32 | ||||
| chr17:77288145-77288284 | Common:1; Rare:32 | ||||
| chr17:77319397-77319668 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:77319691-77319969 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:77320074-77320329 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:78168433-78168635 | Common:1; Rare:56 | ||||
| chr17:78186979-78187386 | Common:3; Rare:141 | ||||
| chr17:78214155-78214334 | Common:3; Rare:67 | ||||
| chr17:78214337-78214425 | Rare:22 | ||||
| chr17:78360160-78360515 | Common:2; Rare:95 | ||||
| chr17:78378594-78378692 | Common:1; Rare:44 |