| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15469731-15469896 | Common:1; Rare:35 | ||||
| chr4:15655295-15655457 | Common:1; Rare:74 | ||||
| chr4:15681458-15681875 | Common:4; Rare:145 | ||||
| chr4:17614553-17614678 | Common:2; Rare:65 | ||||
| chr4:17810562-17811036 | Common:3; Rare:138 | ||||
| chr4:24584381-24584697 | Rare:102 | ||||
| chr4:24795333-24795619 | Common:1; Rare:65 | ||||
| chr4:25160370-25160727 | Common:3; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234096 | Rare:105 | ||||
| chr4:25376956-25377325 | Common:4; Rare:110 | ||||
| chr4:25914051-25914292 | Common:2; Rare:103 | ||||
| chr4:26320480-26320832 | Common:1; Rare:116 | ||||
| chr4:26320905-26321041 | Rare:47; Clinvar (benign):1 | ||||
| chr4:26860548-26860807 | Common:2; Rare:80 | ||||
| chr4:37826577-37826729 | Common:1; Rare:56 |