| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26320900-26321043 | Rare:51; Clinvar (benign):1 | ||||
| chr4:26857678-26857739 | Rare:23 | ||||
| chr4:26860563-26860825 | Common:3; Rare:89 | ||||
| chr4:30720261-30720432 | Rare:44 | ||||
| chr4:30721135-30721443 | Common:3; Rare:78 | ||||
| chr4:37826515-37826748 | Common:6; Rare:89 | ||||
| chr4:37890515-37890672 | Common:1; Rare:34 | ||||
| chr4:37891164-37891257 | Common:2; Rare:32 | ||||
| chr4:37977208-37977459 | Rare:57 | ||||
| chr4:38664229-38664301 | Rare:28 | ||||
| chr4:39182202-39182548 | Rare:75; Clinvar:2 | ||||
| chr4:39458868-39459122 | Common:3; Rare:142; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527405-39527775 | Common:2; Rare:98 | ||||
| chr4:39527959-39528015 | Rare:13 | ||||
| chr4:39638847-39639177 | Common:1; Rare:125 |