| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107824337-107824735 | Common:1; Rare:76 | ||||
| chr4:107989663-107989935 | Common:6; Rare:121; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620380-108620792 | Common:6; Rare:166 | ||||
| chr4:108620805-108620980 | Common:1; Rare:41 | ||||
| chr4:108621648-108622031 | Common:2; Rare:77 | ||||
| chr4:108650266-108650763 | Common:2; Rare:157 | ||||
| chr4:109433757-109433819 | Common:1; Rare:25 | ||||
| chr4:109560068-109560376 | Common:5; Rare:90 | ||||
| chr4:109730057-109730218 | Common:2; Rare:34 | ||||
| chr4:109815410-109815811 | Common:2; Rare:106 | ||||
| chr4:109912765-109912900 | Rare:28; Clinvar:1 | ||||
| chr4:109913004-109913199 | Common:1; Rare:21; Clinvar:3 | ||||
| chr4:110198535-110198669 | Rare:36 | ||||
| chr4:110198720-110198813 | Rare:29 | ||||
| chr4:112231587-112231915 | Common:2; Rare:95 |