| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:164383910-164384179 | Common:1; Rare:56 | ||||
| chr4:164956832-164957006 | Common:2; Rare:60 | ||||
| chr4:165112818-165112973 | Rare:46 | ||||
| chr4:165327295-165327762 | Common:3; Rare:143 | ||||
| chr4:168092483-168092716 | Rare:40 | ||||
| chr4:168831975-168832099 | Common:2; Rare:34 | ||||
| chr4:169010245-169010444 | Common:1; Rare:58 | ||||
| chr4:169612573-169612643 | Common:3; Rare:32; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:169620391-169620718 | Common:2; Rare:113 | ||||
| chr4:169757829-169758059 | Common:2; Rare:77 | ||||
| chr4:173168574-173168838 | Common:2; Rare:82 | ||||
| chr4:173369778-173369935 | Common:1; Rare:51 | ||||
| chr4:173530195-173530462 | Common:2; Rare:61 | ||||
| chr4:174283643-174283965 | Common:1; Rare:61 | ||||
| chr4:174522447-174522617 | Rare:55; Clinvar:2; Clinvar (pathogenic):1 |