| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122921890-122922230 | Common:6; Rare:85 | ||||
| chr4:122922933-122923145 | Common:4; Rare:128; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123396677-123396918 | Rare:56 | ||||
| chr4:123399130-123399584 | Common:10; Rare:186 | ||||
| chr4:124712622-124712905 | Common:2; Rare:164 | ||||
| chr4:127782059-127782351 | Common:2; Rare:79 | ||||
| chr4:127880735-127880947 | Common:2; Rare:150 | ||||
| chr4:127965908-127966017 | Common:1; Rare:18; Clinvar (benign):1 | ||||
| chr4:128060661-128060855 | Common:2; Rare:83 | ||||
| chr4:128061000-128061397 | Common:2; Rare:266 | ||||
| chr4:128287737-128288045 | Common:6; Rare:224 | ||||
| chr4:128288172-128288396 | Common:9; Rare:131 | ||||
| chr4:128811070-128811399 | Rare:116 | ||||
| chr4:128811893-128812340 | Common:4; Rare:248 | ||||
| chr4:129093428-129093728 | Common:3; Rare:160 |