| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41021837-41022450 | Common:7; Rare:310 | ||||
| chr22:41022470-41022930 | Common:7; Rare:238 | ||||
| chr22:41048660-41049124 | Common:1; Rare:135 | ||||
| chr22:41092362-41092674 | Rare:222 | ||||
| chr22:41092890-41093523 | Common:6; Rare:331; Clinvar (benign):1 | ||||
| chr22:41197397-41197716 | Common:4; Rare:143 | ||||
| chr22:41256892-41257215 | Rare:48 | ||||
| chr22:41288344-41288575 | Common:2; Rare:74 | ||||
| chr22:41302564-41302840 | Common:2; Rare:117 | ||||
| chr22:41380987-41381109 | Common:3; Rare:27 | ||||
| chr22:41413310-41413830 | Common:10; Rare:332 | ||||
| chr22:41413833-41414144 | Common:2; Rare:183 | ||||
| chr22:41443936-41444716 | Common:14; Rare:296 | ||||
| chr22:41445059-41445537 | Common:2; Rare:145 | ||||
| chr22:41445864-41446264 | Common:1; Rare:163 |