| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:123396630-123396863 | Rare:61 | ||||
| chr4:123399368-123399653 | Common:1; Rare:89 | ||||
| chr4:127632768-127632968 | Common:1; Rare:50 | ||||
| chr4:128287789-128288016 | Common:3; Rare:88 | ||||
| chr4:128288172-128288396 | Common:5; Rare:80 | ||||
| chr4:128811108-128811320 | Rare:42 | ||||
| chr4:129093444-129093741 | Common:2; Rare:85 | ||||
| chr4:139301299-139301538 | Common:3; Rare:73 | ||||
| chr4:139302463-139302478 | Rare:4 | ||||
| chr4:139302480-139302540 | Rare:9 | ||||
| chr4:139453683-139453760 | Common:2; Rare:26 | ||||
| chr4:139453770-139454263 | Common:3; Rare:140; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556115-139556517 | Rare:85 | ||||
| chr4:140373380-140373701 | Common:2; Rare:129 | ||||
| chr4:140523977-140524222 | Common:2; Rare:73 |