| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122922532-122922689 | Common:2; Rare:72 | ||||
| chr4:122922897-122923184 | Common:2; Rare:84; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:122923349-122923417 | Rare:9 | ||||
| chr4:123396723-123396886 | Rare:44 | ||||
| chr4:127632833-127632971 | Rare:34 | ||||
| chr4:127782180-127782361 | Common:2; Rare:57 | ||||
| chr4:127880759-127880939 | Rare:65 | ||||
| chr4:127965919-127965984 | Common:1; Rare:11; Clinvar (benign):1 | ||||
| chr4:128287479-128287912 | Common:2; Rare:173; Clinvar:1 | ||||
| chr4:128288146-128288364 | Common:6; Rare:78 | ||||
| chr4:128809525-128810286 | Common:4; Rare:221 | ||||
| chr4:128810990-128811091 | Rare:18 | ||||
| chr4:128811121-128811402 | Rare:65 | ||||
| chr4:129093441-129093748 | Common:2; Rare:87 | ||||
| chr4:133149085-133149346 | Common:2; Rare:75 |