| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:6987002-6987303 | Common:2; Rare:96 | ||||
| chr4:7068011-7068347 | Common:5; Rare:113 | ||||
| chr4:8440717-8440918 | Rare:76 | ||||
| chr4:10116650-10117089 | Common:8; Rare:200 | ||||
| chr4:11428892-11429207 | Common:1; Rare:89 | ||||
| chr4:15655295-15655466 | Common:1; Rare:80 | ||||
| chr4:15681458-15681879 | Common:4; Rare:146 | ||||
| chr4:16083690-16083781 | Common:1; Rare:23 | ||||
| chr4:16083969-16084080 | Rare:32 | ||||
| chr4:16898560-16898886 | Common:14; Rare:60 | ||||
| chr4:17577331-17577567 | Rare:112 | ||||
| chr4:17614548-17614678 | Common:2; Rare:68 | ||||
| chr4:17810677-17811080 | Common:4; Rare:126 | ||||
| chr4:24584381-24584744 | Common:1; Rare:110 | ||||
| chr4:25160376-25160676 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 |