| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36387935-36388322 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481567-36481737 | Common:2; Rare:47 | ||||
| chr22:36507031-36507168 | Common:3; Rare:47 | ||||
| chr22:36529077-36529531 | Common:6; Rare:142 | ||||
| chr22:36776046-36776377 | Common:2; Rare:82 | ||||
| chr22:37019416-37019768 | Common:5; Rare:104 | ||||
| chr22:37199366-37199544 | Common:2; Rare:46 | ||||
| chr22:37560296-37560569 | Common:1; Rare:90 | ||||
| chr22:37580035-37580240 | Common:2; Rare:52 | ||||
| chr22:37608679-37609059 | Common:2; Rare:110 | ||||
| chr22:37676072-37676188 | Rare:18 | ||||
| chr22:37807742-37807952 | Common:4; Rare:73 | ||||
| chr22:37849291-37849480 | Rare:113 | ||||
| chr22:37953609-37953755 | Rare:63 | ||||
| chr22:38181728-38182049 | Common:3; Rare:83; Clinvar:1 |