| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88592300-88592542 | Common:1; Rare:75 | ||||
| chr4:88697693-88697924 | Common:2; Rare:86 | ||||
| chr4:88823051-88823376 | Common:4; Rare:59 | ||||
| chr4:89057115-89057222 | Common:1; Rare:22 | ||||
| chr4:89111075-89111180 | Rare:21 | ||||
| chr4:89111322-89111644 | Common:4; Rare:113 | ||||
| chr4:89837048-89837423 | Common:5; Rare:124; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:90127283-90127599 | Common:1; Rare:106 | ||||
| chr4:90649368-90649527 | Common:1; Rare:25 | ||||
| chr4:92822848-92822974 | Common:4; Rare:24 | ||||
| chr4:94207541-94207988 | Common:2; Rare:135 | ||||
| chr4:94451798-94451993 | Common:3; Rare:61 | ||||
| chr4:94757689-94758053 | Common:4; Rare:109 | ||||
| chr4:95548742-95549559 | Common:5; Rare:225 | ||||
| chr4:95840054-95840151 | Common:3; Rare:44 |