| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:87006876-87007422 | Common:5; Rare:182 | ||||
| chr4:87390861-87391368 | Common:5; Rare:173 | ||||
| chr4:87422507-87422898 | Common:2; Rare:109 | ||||
| chr4:87529043-87529524 | Common:5; Rare:85 | ||||
| chr4:87531026-87531192 | Rare:32 | ||||
| chr4:88158565-88158770 | Rare:54 | ||||
| chr4:88284540-88284941 | Common:2; Rare:98 | ||||
| chr4:88523598-88523864 | Common:2; Rare:90 | ||||
| chr4:88592293-88592535 | Common:1; Rare:74 | ||||
| chr4:88697741-88697905 | Common:1; Rare:62 | ||||
| chr4:88823122-88823388 | Common:3; Rare:48 | ||||
| chr4:89111371-89111644 | Common:3; Rare:96 | ||||
| chr4:89836913-89837244 | Common:3; Rare:106; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:94207836-94207942 | Rare:42 | ||||
| chr4:94451792-94451993 | Common:3; Rare:64 |