| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:6640549-6640715 | Common:2; Rare:67 | ||||
| chr4:6987034-6987292 | Common:1; Rare:82 | ||||
| chr4:7068037-7068392 | Common:7; Rare:121 | ||||
| chr4:8436022-8436158 | Common:1; Rare:23 | ||||
| chr4:8440717-8440975 | Rare:98 | ||||
| chr4:15655295-15655457 | Common:1; Rare:74 | ||||
| chr4:15681458-15681863 | Common:3; Rare:141 | ||||
| chr4:16898590-16898864 | Common:14; Rare:43 | ||||
| chr4:17614555-17614651 | Common:2; Rare:40 | ||||
| chr4:17810687-17811056 | Common:4; Rare:116 | ||||
| chr4:25160418-25160670 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914051-25914310 | Common:2; Rare:111 | ||||
| chr4:26320450-26320826 | Common:1; Rare:114 | ||||
| chr4:26320900-26321028 | Rare:45; Clinvar (benign):1 | ||||
| chr4:37826532-37826729 | Common:6; Rare:71 |