| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:124712721-124712909 | Rare:60 | ||||
| chr4:124712943-124713135 | Common:1; Rare:48 | ||||
| chr4:127622770-127623050 | Common:1; Rare:51 | ||||
| chr4:127632792-127633040 | Common:1; Rare:72 | ||||
| chr4:127782141-127782361 | Common:2; Rare:63 | ||||
| chr4:127782537-127782852 | Common:1; Rare:73 | ||||
| chr4:127783200-127783570 | Common:1; Rare:72 | ||||
| chr4:127880711-127880953 | Common:1; Rare:84 | ||||
| chr4:127881464-127881602 | Rare:30 | ||||
| chr4:127965110-127965406 | Rare:97; Clinvar:5; Clinvar (benign):2 | ||||
| chr4:128061065-128061352 | Common:1; Rare:104 | ||||
| chr4:128286562-128287148 | Common:4; Rare:201 | ||||
| chr4:128287155-128287555 | Common:1; Rare:254 | ||||
| chr4:128287769-128288366 | Common:9; Rare:207 | ||||
| chr4:128809562-128809815 | Common:1; Rare:78 |