| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75979386-75979611 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr17:76103712-76103898 | Common:5; Rare:61 | ||||
| chr17:76264872-76265203 | Common:1; Rare:78 | ||||
| chr17:76353621-76353985 | Common:2; Rare:130 | ||||
| chr17:76709184-76709513 | Rare:58 | ||||
| chr17:76725747-76726086 | Common:1; Rare:95 | ||||
| chr17:76726458-76726903 | Common:5; Rare:172 | ||||
| chr17:76737319-76737687 | Common:4; Rare:129 | ||||
| chr17:76737845-76738084 | Common:3; Rare:69 | ||||
| chr17:77088585-77088795 | Common:1; Rare:60 | ||||
| chr17:77140529-77141045 | Common:5; Rare:180 | ||||
| chr17:77374432-77374435 | |||||
| chr17:77374440-77374618 | Rare:44 | ||||
| chr17:77450471-77450785 | Rare:64 | ||||
| chr17:78168453-78168611 | Rare:41 |