| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37634482-37634707 | Rare:47 | ||||
| chr22:37675384-37675710 | Common:4; Rare:95 | ||||
| chr22:37849300-37849480 | Rare:107 | ||||
| chr22:37953587-37953765 | Rare:76 | ||||
| chr22:38181728-38182024 | Common:3; Rare:78; Clinvar:1 | ||||
| chr22:38398469-38398587 | Rare:42 | ||||
| chr22:38505656-38505958 | Rare:106 | ||||
| chr22:38505980-38506035 | Rare:21 | ||||
| chr22:38506087-38506193 | Rare:27 | ||||
| chr22:38506197-38506580 | Common:1; Rare:139 | ||||
| chr22:38570184-38570500 | Common:5; Rare:57 | ||||
| chr22:38656370-38656716 | Common:1; Rare:87 | ||||
| chr22:38681810-38682019 | Common:2; Rare:91 | ||||
| chr22:38739356-38739501 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:38742513-38742637 | Common:1; Rare:44 |