| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123584592-123585720 | Common:19; Rare:945 | ||||
| chr3:123883999-123884651 | Common:11; Rare:322; Clinvar:6; Clinvar (benign):4 | ||||
| chr3:123960369-123961077 | Common:3; Rare:137 | ||||
| chr3:123961143-123961678 | Common:12; Rare:573 | ||||
| chr3:124584410-124584840 | Common:6; Rare:246 | ||||
| chr3:124584862-124585343 | Common:3; Rare:188 | ||||
| chr3:124730210-124730530 | Common:20; Rare:591; Clinvar:18; Clinvar (benign):18 | ||||
| chr3:124878745-124879188 | Common:12; Rare:135 | ||||
| chr3:124886635-124887035 | Common:3; Rare:94 | ||||
| chr3:124887180-124887930 | Common:9; Rare:502 | ||||
| chr3:125056011-125056263 | Rare:123 | ||||
| chr3:125154679-125155079 | Common:6; Rare:161 | ||||
| chr3:125374585-125375259 | Rare:258 | ||||
| chr3:125375223-125375623 | Common:4; Rare:424 | ||||
| chr3:125520067-125520467 | Rare:440 |