| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158671868-158672453 | Common:5; Rare:148; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:164956895-164957008 | Rare:36 | ||||
| chr4:168893700-168893988 | Common:1; Rare:65 | ||||
| chr4:169620385-169620604 | Common:2; Rare:84 | ||||
| chr4:173370681-173370976 | Common:2; Rare:76 | ||||
| chr4:174283130-174283332 | Rare:30 | ||||
| chr4:174283612-174283964 | Common:1; Rare:71 | ||||
| chr4:174522467-174522613 | Rare:48; Clinvar:2 | ||||
| chr4:177442376-177442521 | Rare:87; Clinvar:2 | ||||
| chr4:182917291-182917558 | Common:4; Rare:85 | ||||
| chr4:183504523-183504810 | Common:2; Rare:94 | ||||
| chr4:183659040-183659401 | Common:1; Rare:110 | ||||
| chr4:184474504-184474817 | Rare:70 | ||||
| chr4:184649403-184649783 | Common:4; Rare:127 | ||||
| chr4:184805355-184805828 | Common:2; Rare:89 |