| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25160360-25160727 | Common:3; Rare:112; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233835-25234131 | Rare:113 | ||||
| chr4:25863532-25863653 | Rare:24 | ||||
| chr4:25914051-25914321 | Common:2; Rare:115 | ||||
| chr4:26860568-26860807 | Common:1; Rare:78 | ||||
| chr4:37583927-37584362 | Common:3; Rare:72 | ||||
| chr4:37826579-37826735 | Common:1; Rare:59 | ||||
| chr4:37977168-37977459 | Rare:69 | ||||
| chr4:38664211-38664301 | Rare:32 | ||||
| chr4:38914676-38914944 | Common:1; Rare:41 | ||||
| chr4:39182334-39182548 | Rare:48; Clinvar:2 | ||||
| chr4:39458857-39459120 | Common:3; Rare:152; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527353-39527795 | Common:3; Rare:119 | ||||
| chr4:39638829-39639149 | Common:1; Rare:118 | ||||
| chr4:39697933-39698268 | Common:2; Rare:136 |