| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26320589-26320832 | Common:1; Rare:92 | ||||
| chr4:26320904-26321041 | Rare:48; Clinvar (benign):1 | ||||
| chr4:26583886-26584153 | Rare:57 | ||||
| chr4:26857519-26857771 | Common:4; Rare:79 | ||||
| chr4:26860563-26860812 | Common:2; Rare:81 | ||||
| chr4:30720237-30720422 | Common:1; Rare:48 | ||||
| chr4:37826571-37826735 | Common:1; Rare:61 | ||||
| chr4:38664211-38664291 | Rare:26 | ||||
| chr4:38856773-38856955 | Common:5; Rare:27 | ||||
| chr4:38867588-38867826 | Common:2; Rare:84 | ||||
| chr4:39182267-39182548 | Rare:64; Clinvar:2 | ||||
| chr4:39366315-39366456 | Rare:43 | ||||
| chr4:39458593-39459134 | Common:6; Rare:216; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527282-39527789 | Common:6; Rare:136 | ||||
| chr4:39527925-39528027 | Rare:24 |