| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38258052-38258208 | Common:2; Rare:26 | ||||
| chr22:38424158-38424314 | Common:1; Rare:29 | ||||
| chr22:39468874-39469030 | Rare:33 | ||||
| chr22:39469076-39469300 | Rare:52 | ||||
| chr22:39521644-39521813 | Common:1; Rare:81 | ||||
| chr22:40877560-40877938 | Common:2; Rare:72 | ||||
| chr22:41021971-41022039 | Rare:18 | ||||
| chr22:41129967-41130226 | Rare:47 | ||||
| chr22:41256020-41256221 | Rare:66 | ||||
| chr22:41414533-41414699 | Rare:31 | ||||
| chr22:41471617-41471850 | Rare:34 | ||||
| chr22:41522821-41523240 | Rare:115; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr22:41524681-41524905 | Rare:62 | ||||
| chr22:41658049-41658309 | Common:3; Rare:48 | ||||
| chr22:42126955-42127223 | Common:3; Rare:92 |