| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:153344567-153344738 | Common:4; Rare:52 | ||||
| chr4:153466088-153466388 | Common:3; Rare:117 | ||||
| chr4:154550327-154550492 | Common:1; Rare:56 | ||||
| chr4:156970884-156971199 | Rare:54 | ||||
| chr4:156971797-156971983 | Common:1; Rare:71 | ||||
| chr4:158671849-158672162 | Common:4; Rare:81; Clinvar:1 | ||||
| chr4:158672208-158672385 | Common:1; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723279-158723463 | Common:2; Rare:82 | ||||
| chr4:163166832-163167001 | Common:2; Rare:61 | ||||
| chr4:163494432-163494758 | Common:2; Rare:129 | ||||
| chr4:164956891-164957016 | Common:1; Rare:40 | ||||
| chr4:164977616-164977706 | Rare:23 | ||||
| chr4:165327411-165327755 | Common:2; Rare:101 | ||||
| chr4:168480471-168480536 | Rare:14 | ||||
| chr4:169010113-169010335 | Common:6; Rare:79 |