| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38952609-38952774 | Rare:24 | ||||
| chr22:38957406-38957612 | Rare:39 | ||||
| chr22:39319596-39319752 | Common:3; Rare:75 | ||||
| chr22:39502162-39502397 | Rare:66 | ||||
| chr22:40044121-40044341 | Common:2; Rare:50 | ||||
| chr22:40044528-40044868 | Common:2; Rare:79 | ||||
| chr22:40346441-40346556 | Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40636659-40637014 | Common:2; Rare:96 | ||||
| chr22:40856727-40857154 | Common:2; Rare:159; Clinvar:3 | ||||
| chr22:40951031-40951417 | Common:2; Rare:134 | ||||
| chr22:41446785-41446980 | Rare:84 | ||||
| chr22:41560884-41561172 | Common:9; Rare:80 | ||||
| chr22:41589778-41589872 | Common:1; Rare:49 | ||||
| chr22:41621018-41621399 | Common:7; Rare:142 | ||||
| chr22:41800517-41800631 | Rare:37 |