| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:110198535-110198866 | Rare:95 | ||||
| chr4:112231534-112231852 | Common:2; Rare:107 | ||||
| chr4:112285851-112285978 | Rare:40 | ||||
| chr4:112636853-112637187 | Common:1; Rare:93 | ||||
| chr4:113979578-113979869 | Common:6; Rare:63 | ||||
| chr4:118685339-118685541 | Common:2; Rare:57 | ||||
| chr4:118835990-118836227 | Common:1; Rare:55 | ||||
| chr4:119212472-119212730 | Common:2; Rare:76 | ||||
| chr4:120066754-120066964 | Common:4; Rare:62 | ||||
| chr4:121696843-121697159 | Common:5; Rare:84 | ||||
| chr4:121823499-121823539 | Rare:12 | ||||
| chr4:122732425-122732776 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:122922897-122923144 | Common:2; Rare:73; Clinvar (pathogenic):1 | ||||
| chr4:123399348-123399540 | Common:1; Rare:56 | ||||
| chr4:124712128-124712298 | Rare:42 |