| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:155208696-155208874 | Rare:36 | ||||
| chr4:155667293-155667430 | Rare:28 | ||||
| chr4:158172354-158172535 | Rare:27 | ||||
| chr4:158172564-158172856 | Common:1; Rare:51 | ||||
| chr4:158172978-158173237 | Rare:42 | ||||
| chr4:158671849-158672427 | Common:5; Rare:152; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723294-158723463 | Common:2; Rare:77 | ||||
| chr4:163166832-163166979 | Common:2; Rare:52 | ||||
| chr4:165327400-165327734 | Common:2; Rare:97 | ||||
| chr4:168831907-168832175 | Common:3; Rare:77 | ||||
| chr4:169010233-169010428 | Common:1; Rare:59 | ||||
| chr4:169620390-169620719 | Common:2; Rare:113 | ||||
| chr4:169757853-169757997 | Rare:48 | ||||
| chr4:173369732-173369964 | Common:1; Rare:75 | ||||
| chr4:173370674-173371012 | Common:2; Rare:87 |