| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:17969465-17969544 | Rare:12 | ||||
| chr20:17969891-17970109 | Common:1; Rare:68; Clinvar (benign):3 | ||||
| chr20:18137666-18138180 | Common:3; Rare:172 | ||||
| chr20:18138497-18138595 | Rare:26 | ||||
| chr20:18288099-18288618 | Common:3; Rare:134 | ||||
| chr20:18413192-18413480 | Rare:43 | ||||
| chr20:18466729-18467110 | Rare:84 | ||||
| chr20:18467171-18467526 | Common:3; Rare:83 | ||||
| chr20:18496698-18497006 | Common:1; Rare:54 | ||||
| chr20:18497173-18497378 | Common:2; Rare:66 | ||||
| chr20:18507308-18507636 | Common:1; Rare:87; Clinvar:1 | ||||
| chr20:18507719-18508016 | Common:3; Rare:95; Clinvar:5; Clinvar (benign):3 | ||||
| chr20:18567173-18567643 | Common:4; Rare:150 | ||||
| chr20:18587772-18588211 | Common:3; Rare:113 | ||||
| chr20:18588344-18588478 | Rare:27 |