| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:35299587-35299967 | Common:3; Rare:98 | ||||
| chr22:35399903-35400201 | Rare:103 | ||||
| chr22:35637857-35638098 | Common:1; Rare:51 | ||||
| chr22:36253007-36253111 | Rare:24 | ||||
| chr22:36365139-36365193 | Rare:13 | ||||
| chr22:36387975-36388371 | Common:3; Rare:110; Clinvar (benign):1 | ||||
| chr22:36481204-36481668 | Common:4; Rare:121 | ||||
| chr22:36506811-36506866 | Common:1; Rare:8 | ||||
| chr22:36507024-36507198 | Common:3; Rare:66 | ||||
| chr22:36528866-36529544 | Common:6; Rare:214 | ||||
| chr22:36817114-36817230 | Common:1; Rare:32 | ||||
| chr22:37007766-37007954 | Common:1; Rare:30 | ||||
| chr22:37199338-37199684 | Common:6; Rare:105 | ||||
| chr22:37212017-37212235 | Common:4; Rare:46 | ||||
| chr22:37212357-37212598 | Common:1; Rare:40 |