| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:18021657-18021920 | Common:2; Rare:137 | ||||
| chr4:20700322-20700495 | Common:1; Rare:75 | ||||
| chr4:24584472-24584718 | Common:1; Rare:77 | ||||
| chr4:25160385-25160728 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25377002-25377325 | Common:3; Rare:98 | ||||
| chr4:25914051-25914358 | Common:3; Rare:131 | ||||
| chr4:26320592-26320832 | Common:1; Rare:92 | ||||
| chr4:26320905-26321041 | Rare:47; Clinvar (benign):1 | ||||
| chr4:26860607-26860798 | Common:1; Rare:62 | ||||
| chr4:37826413-37826773 | Common:8; Rare:124 | ||||
| chr4:37977202-37977454 | Rare:59 | ||||
| chr4:38867666-38867822 | Common:1; Rare:63 | ||||
| chr4:39366319-39366416 | Rare:30 | ||||
| chr4:39458641-39459122 | Common:6; Rare:198; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527359-39527761 | Common:2; Rare:97 |