| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36387843-36388322 | Common:4; Rare:241; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:36481520-36481668 | Common:2; Rare:100 | ||||
| chr22:36481940-36482234 | Common:4; Rare:135 | ||||
| chr22:36506980-36507168 | Common:6; Rare:110 | ||||
| chr22:36529092-36529541 | Common:12; Rare:263 | ||||
| chr22:37018796-37019196 | Common:2; Rare:117 | ||||
| chr22:37019390-37019868 | Common:10; Rare:273 | ||||
| chr22:37051595-37051769 | Common:2; Rare:46 | ||||
| chr22:37199250-37199735 | Common:14; Rare:234 | ||||
| chr22:37486326-37486471 | Rare:95 | ||||
| chr22:37519204-37520002 | Common:6; Rare:253 | ||||
| chr22:37560331-37560540 | Common:2; Rare:128 | ||||
| chr22:37563340-37563780 | Common:4; Rare:146 | ||||
| chr22:37579916-37580082 | Common:2; Rare:81 | ||||
| chr22:37608427-37608545 | Common:2; Rare:80 |