| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:153788572-153789224 | Common:4; Rare:215 | ||||
| chr4:154550347-154550568 | Common:1; Rare:77 | ||||
| chr4:156970880-156971214 | Rare:57 | ||||
| chr4:158172360-158172740 | Rare:63 | ||||
| chr4:158172986-158173172 | Rare:32 | ||||
| chr4:158671825-158672313 | Common:5; Rare:124; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723319-158723484 | Common:2; Rare:76 | ||||
| chr4:165327411-165327741 | Common:2; Rare:95 | ||||
| chr4:168480437-168480797 | Common:1; Rare:58 | ||||
| chr4:168921238-168921738 | Common:2; Rare:94; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:169010223-169010490 | Common:1; Rare:85 | ||||
| chr4:169612569-169612794 | Common:4; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:169620406-169620723 | Common:2; Rare:105 | ||||
| chr4:173168620-173168838 | Common:2; Rare:72 | ||||
| chr4:173333502-173333861 | Common:2; Rare:94 |