| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37826534-37826729 | Common:6; Rare:70 | ||||
| chr4:38664841-38665018 | Rare:57 | ||||
| chr4:39458826-39459120 | Common:3; Rare:160; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527422-39527728 | Common:2; Rare:76 | ||||
| chr4:39638858-39639140 | Common:1; Rare:106 | ||||
| chr4:39698051-39698197 | Common:1; Rare:57 | ||||
| chr4:40056645-40056951 | Common:4; Rare:94 | ||||
| chr4:40197047-40197158 | Rare:15 | ||||
| chr4:40749868-40750003 | Rare:40 | ||||
| chr4:41360680-41360815 | Common:1; Rare:39 | ||||
| chr4:41990388-41990573 | Common:1; Rare:67 | ||||
| chr4:44726498-44726644 | Common:1; Rare:52 | ||||
| chr4:47485204-47485353 | Common:1; Rare:55 | ||||
| chr4:47914569-47914682 | Common:1; Rare:38 | ||||
| chr4:48269779-48270021 | Common:2; Rare:59 |