| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127672700-127672998 | Common:4; Rare:133 | ||||
| chr3:127823170-127823449 | Common:4; Rare:54 | ||||
| chr3:128052139-128052569 | Common:4; Rare:143 | ||||
| chr3:128087638-128087786 | Rare:32 | ||||
| chr3:128123690-128124039 | Rare:102 | ||||
| chr3:128153388-128153491 | Rare:28 | ||||
| chr3:128650763-128651105 | Common:2; Rare:100 | ||||
| chr3:128680633-128680800 | Common:2; Rare:47 | ||||
| chr3:128681108-128681243 | Common:1; Rare:38 | ||||
| chr3:128725975-128726233 | Common:1; Rare:78; Clinvar:3 | ||||
| chr3:128726333-128726343 | Common:1; Rare:1; Clinvar (benign):1 | ||||
| chr3:128879357-128879704 | Common:5; Rare:163; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129161004-129161477 | Common:2; Rare:150 | ||||
| chr3:129183814-129184123 | Common:2; Rare:118 | ||||
| chr3:129249536-129249746 | Common:1; Rare:58 |