| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25863563-25863668 | Rare:19 | ||||
| chr4:25914051-25914340 | Common:3; Rare:124 | ||||
| chr4:26319444-26319746 | Rare:91 | ||||
| chr4:26320743-26320881 | Rare:69 | ||||
| chr4:26320905-26321046 | Rare:51; Clinvar (benign):1 | ||||
| chr4:26857519-26857753 | Common:4; Rare:72 | ||||
| chr4:26860568-26860819 | Common:2; Rare:85 | ||||
| chr4:37453873-37453976 | Rare:34 | ||||
| chr4:37584108-37584362 | Common:1; Rare:44 | ||||
| chr4:37826577-37826730 | Common:1; Rare:57 | ||||
| chr4:37977200-37977459 | Rare:61 | ||||
| chr4:38664211-38664291 | Rare:26 | ||||
| chr4:38867567-38867846 | Common:2; Rare:92 | ||||
| chr4:39366270-39366431 | Common:1; Rare:49 | ||||
| chr4:39458856-39459116 | Common:3; Rare:150; Clinvar (benign):5 |