| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37676035-37676300 | Common:3; Rare:56 | ||||
| chr22:37686563-37686638 | Rare:13 | ||||
| chr22:37746024-37746420 | Common:5; Rare:132; Clinvar (benign):1 | ||||
| chr22:37805571-37805816 | Rare:78 | ||||
| chr22:37807670-37808066 | Common:4; Rare:143 | ||||
| chr22:37849278-37849481 | Rare:123 | ||||
| chr22:37932660-37932847 | Common:1; Rare:60 | ||||
| chr22:37953544-37953788 | Rare:95 | ||||
| chr22:38201771-38202119 | Common:2; Rare:98 | ||||
| chr22:38272910-38273169 | Common:2; Rare:105 | ||||
| chr22:38294109-38294525 | Rare:158 | ||||
| chr22:38317160-38317545 | Common:3; Rare:149 | ||||
| chr22:38318419-38318534 | Rare:26 | ||||
| chr22:38494756-38494975 | Rare:35 | ||||
| chr22:38506129-38506637 | Common:1; Rare:172 |