| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123585489-123585553 | Rare:11 | ||||
| chr3:123700963-123701321 | Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:124730387-124730485 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:125375118-125375384 | Rare:67 | ||||
| chr3:125520129-125520299 | Rare:61 | ||||
| chr3:126704114-126704294 | Common:2; Rare:53 | ||||
| chr3:127598220-127598458 | Common:3; Rare:70 | ||||
| chr3:127628903-127629287 | Common:1; Rare:124 | ||||
| chr3:127672808-127672992 | Common:2; Rare:84 | ||||
| chr3:128052171-128052500 | Common:2; Rare:110 | ||||
| chr3:128725954-128726202 | Common:1; Rare:66; Clinvar:2 | ||||
| chr3:128879425-128879669 | Common:4; Rare:120; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183814-129184075 | Common:2; Rare:89 | ||||
| chr3:129249534-129249675 | Common:1; Rare:44 | ||||
| chr3:129278762-129278892 | Common:4; Rare:43 |