| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33686318-33686757 | Common:3; Rare:114 | ||||
| chr20:33719868-33719905 | Rare:15 | ||||
| chr20:33720075-33720188 | Rare:45 | ||||
| chr20:33720204-33720565 | Common:4; Rare:92 | ||||
| chr20:33731816-33732056 | Common:1; Rare:74 | ||||
| chr20:33732235-33732608 | Common:4; Rare:81 | ||||
| chr20:33811055-33811480 | Common:1; Rare:124 | ||||
| chr20:33993021-33993416 | Common:1; Rare:93 | ||||
| chr20:33993853-33994048 | Rare:81 | ||||
| chr20:33994142-33994309 | Rare:46 | ||||
| chr20:33994356-33994638 | Common:2; Rare:78 | ||||
| chr20:34111748-34111898 | Rare:38 | ||||
| chr20:34112206-34112514 | Common:1; Rare:97 | ||||
| chr20:34302918-34303160 | Rare:77 | ||||
| chr20:34303254-34303567 | Common:2; Rare:116; Clinvar:3; Clinvar (benign):2 |