| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15655289-15655473 | Common:1; Rare:83 | ||||
| chr4:15681420-15681875 | Common:4; Rare:152 | ||||
| chr4:16083678-16083890 | Common:2; Rare:65 | ||||
| chr4:17614529-17614651 | Common:2; Rare:48 | ||||
| chr4:17810687-17811025 | Common:3; Rare:103 | ||||
| chr4:20700270-20700499 | Common:1; Rare:100 | ||||
| chr4:23890042-23890132 | Rare:12 | ||||
| chr4:25160370-25160609 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233843-25234058 | Rare:92 | ||||
| chr4:25914029-25914308 | Common:2; Rare:121 | ||||
| chr4:26320590-26320843 | Common:1; Rare:98 | ||||
| chr4:26320946-26321041 | Rare:39 | ||||
| chr4:26584004-26584146 | Rare:27 | ||||
| chr4:37826418-37826744 | Common:8; Rare:109 | ||||
| chr4:38867663-38867826 | Common:1; Rare:64 |