| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17614577-17614657 | Common:1; Rare:37 | ||||
| chr4:17810687-17811006 | Common:2; Rare:98 | ||||
| chr4:23889910-23890149 | Rare:43 | ||||
| chr4:24584375-24584716 | Common:1; Rare:106 | ||||
| chr4:24795348-24795619 | Common:1; Rare:64 | ||||
| chr4:25160413-25160727 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914051-25914340 | Common:3; Rare:124 | ||||
| chr4:26320458-26320832 | Common:1; Rare:119 | ||||
| chr4:26320901-26321043 | Rare:50; Clinvar (benign):1 | ||||
| chr4:37826401-37826748 | Common:8; Rare:116 | ||||
| chr4:37890543-37890639 | Rare:16 | ||||
| chr4:37890992-37891244 | Common:2; Rare:76 | ||||
| chr4:37977195-37977470 | Rare:69 | ||||
| chr4:38664214-38664312 | Rare:31 | ||||
| chr4:38867576-38867833 | Common:2; Rare:87 |