| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:155953855-155953935 | Rare:21 | ||||
| chr4:156970563-156970737 | Common:1; Rare:39 | ||||
| chr4:156971123-156971202 | Rare:10 | ||||
| chr4:156971797-156972064 | Common:2; Rare:93 | ||||
| chr4:158172360-158172862 | Common:1; Rare:82 | ||||
| chr4:158172892-158173195 | Rare:44 | ||||
| chr4:158210212-158210568 | Common:3; Rare:88 | ||||
| chr4:158671803-158672453 | Common:5; Rare:176; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723204-158723445 | Common:2; Rare:105 | ||||
| chr4:158805755-158805887 | Common:1; Rare:22 | ||||
| chr4:159103806-159104132 | Common:4; Rare:114 | ||||
| chr4:159228184-159228328 | Rare:31 | ||||
| chr4:159229225-159229472 | Common:2; Rare:40 | ||||
| chr4:163166856-163167009 | Common:2; Rare:56 | ||||
| chr4:163494438-163494741 | Common:2; Rare:118 |