| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:151409339-151409443 | Common:1; Rare:20 | ||||
| chr4:152536044-152536443 | Common:3; Rare:148 | ||||
| chr4:152779715-152780158 | Common:2; Rare:114 | ||||
| chr4:152936135-152936391 | Common:4; Rare:67 | ||||
| chr4:153788910-153789205 | Rare:85 | ||||
| chr4:156971057-156971280 | Common:1; Rare:38 | ||||
| chr4:156971788-156971942 | Common:1; Rare:57 | ||||
| chr4:158172354-158172667 | Rare:49 | ||||
| chr4:158172981-158173219 | Rare:36 | ||||
| chr4:158210230-158210575 | Common:3; Rare:88 | ||||
| chr4:158671849-158672427 | Common:5; Rare:152; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:159103967-159104105 | Common:1; Rare:46 | ||||
| chr4:163166828-163166969 | Common:2; Rare:45 | ||||
| chr4:165327365-165327741 | Common:3; Rare:114 | ||||
| chr4:168317981-168318343 | Common:3; Rare:60 |