| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15469630-15469903 | Common:1; Rare:55 | ||||
| chr4:15655270-15655466 | Common:2; Rare:87 | ||||
| chr4:15681466-15681875 | Common:4; Rare:142 | ||||
| chr4:15703005-15703140 | Common:1; Rare:28 | ||||
| chr4:16898490-16898880 | Common:14; Rare:74 | ||||
| chr4:17614548-17614664 | Common:2; Rare:51 | ||||
| chr4:17810677-17811025 | Common:3; Rare:107 | ||||
| chr4:23890045-23890179 | Rare:20 | ||||
| chr4:24584341-24584725 | Common:1; Rare:117 | ||||
| chr4:25160344-25160727 | Common:3; Rare:116; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233843-25234081 | Rare:101 | ||||
| chr4:25914022-25914292 | Common:3; Rare:118 | ||||
| chr4:26319420-26319760 | Rare:95 | ||||
| chr4:26320874-26321046 | Rare:60; Clinvar (benign):1 | ||||
| chr4:26860624-26860819 | Common:2; Rare:67 |