| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139084278-139084583 | Common:4; Rare:127 | ||||
| chr4:139177183-139177456 | Rare:79 | ||||
| chr4:139301263-139301779 | Common:5; Rare:158 | ||||
| chr4:139302435-139302552 | Rare:27 | ||||
| chr4:139453665-139453712 | Common:1; Rare:18 | ||||
| chr4:139453774-139454204 | Common:3; Rare:112; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556115-139556369 | Rare:63 | ||||
| chr4:139556388-139556557 | Rare:21 | ||||
| chr4:140154086-140154288 | Common:1; Rare:81 | ||||
| chr4:140373374-140373717 | Common:3; Rare:137 | ||||
| chr4:140756144-140756500 | Common:1; Rare:75 | ||||
| chr4:141220770-141221007 | Rare:79 | ||||
| chr4:141636218-141636260 | Rare:8 | ||||
| chr4:141636475-141636662 | Common:1; Rare:37 | ||||
| chr4:141636755-141637001 | Common:1; Rare:55 |