| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17810687-17811080 | Common:4; Rare:122 | ||||
| chr4:20700295-20700551 | Common:3; Rare:109 | ||||
| chr4:24584463-24584725 | Common:1; Rare:79 | ||||
| chr4:25160396-25160725 | Common:3; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25233972 | Rare:49 | ||||
| chr4:25376948-25377315 | Common:4; Rare:110 | ||||
| chr4:25914036-25914318 | Common:2; Rare:121 | ||||
| chr4:26320612-26320832 | Common:1; Rare:90 | ||||
| chr4:26320917-26321046 | Rare:47 | ||||
| chr4:26583866-26584143 | Rare:61 | ||||
| chr4:30719855-30720121 | Common:2; Rare:49 | ||||
| chr4:30720237-30720432 | Common:1; Rare:50 | ||||
| chr4:30721978-30722134 | Common:1; Rare:51 | ||||
| chr4:37243984-37244187 | Common:3; Rare:39 | ||||
| chr4:37826538-37826729 | Common:6; Rare:68 |