| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41301273-41301610 | Common:1; Rare:93 | ||||
| chr22:41446784-41447065 | Common:1; Rare:125 | ||||
| chr22:41468908-41469142 | Rare:62 | ||||
| chr22:41544449-41544876 | Common:5; Rare:113 | ||||
| chr22:41560908-41561082 | Common:8; Rare:51 | ||||
| chr22:41589794-41590172 | Common:6; Rare:136 | ||||
| chr22:41620999-41621377 | Common:7; Rare:138 | ||||
| chr22:41621530-41621606 | Rare:23 | ||||
| chr22:41621620-41621800 | Common:2; Rare:56 | ||||
| chr22:41800536-41800688 | Common:1; Rare:46 | ||||
| chr22:41832904-41833221 | Common:3; Rare:104 | ||||
| chr22:42070770-42070956 | Common:2; Rare:40 | ||||
| chr22:42079590-42079738 | Common:1; Rare:42 | ||||
| chr22:42090643-42090953 | Common:2; Rare:137; Clinvar (pathogenic):1 | ||||
| chr22:42614824-42615251 | Common:3; Rare:186 |