| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:138242222-138242538 | Common:1; Rare:69 | ||||
| chr4:139015462-139015844 | Common:2; Rare:129 | ||||
| chr4:139083904-139083986 | Rare:12 | ||||
| chr4:139084168-139084471 | Common:4; Rare:131 | ||||
| chr4:139177062-139177392 | Rare:84 | ||||
| chr4:139280099-139280347 | Common:1; Rare:71 | ||||
| chr4:139301177-139301609 | Common:6; Rare:119 | ||||
| chr4:139302279-139302578 | Common:3; Rare:68 | ||||
| chr4:139453679-139453829 | Common:2; Rare:46; Clinvar:1 | ||||
| chr4:139453910-139454198 | Common:3; Rare:80; Clinvar:6; Clinvar (benign):4 | ||||
| chr4:139556369-139556622 | Rare:38 | ||||
| chr4:140373319-140373713 | Common:3; Rare:153 | ||||
| chr4:140523987-140524276 | Common:1; Rare:87 | ||||
| chr4:141220794-141220978 | Rare:64 | ||||
| chr4:143184695-143185007 | Common:8; Rare:122 |