| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:126180514-126180658 | Rare:28 | ||||
| chr3:126180879-126180942 | Rare:17 | ||||
| chr3:127598223-127598428 | Common:3; Rare:51 | ||||
| chr3:127628949-127629221 | Common:1; Rare:91 | ||||
| chr3:127672808-127673018 | Common:4; Rare:101 | ||||
| chr3:127822473-127822777 | Rare:69 | ||||
| chr3:128052149-128052555 | Common:3; Rare:138 | ||||
| chr3:128153356-128153518 | Rare:48 | ||||
| chr3:128650540-128650913 | Common:2; Rare:154 | ||||
| chr3:128879421-128879669 | Common:4; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183758-129184075 | Common:2; Rare:108 | ||||
| chr3:129249503-129249698 | Common:3; Rare:58 | ||||
| chr3:129278743-129278900 | Common:4; Rare:45 | ||||
| chr3:129316242-129316391 | Common:1; Rare:57 | ||||
| chr3:129439839-129440371 | Common:1; Rare:162; Clinvar:2; Clinvar (benign):1 |