| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128726048-128726232 | Common:1; Rare:52; Clinvar:3 | ||||
| chr3:128879404-128879685 | Common:4; Rare:139; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:129183794-129184123 | Common:2; Rare:124 | ||||
| chr3:129249463-129249725 | Common:3; Rare:76 | ||||
| chr3:129439869-129440107 | Rare:75 | ||||
| chr3:129560400-129560679 | Rare:79 | ||||
| chr3:129893567-129893875 | Rare:129 | ||||
| chr3:130746760-130747044 | Common:3; Rare:75 | ||||
| chr3:130893898-130894242 | Common:3; Rare:101 | ||||
| chr3:131026740-131026951 | Common:2; Rare:53 | ||||
| chr3:131381529-131381831 | Common:2; Rare:78 | ||||
| chr3:132659799-132659950 | Common:3; Rare:35 | ||||
| chr3:133661863-133662008 | Rare:34 | ||||
| chr3:134374400-134374698 | Common:1; Rare:89 | ||||
| chr3:134485679-134485766 | Rare:34 |