| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:125520163-125520355 | Rare:51 | ||||
| chr3:126704047-126704294 | Common:3; Rare:75 | ||||
| chr3:127598202-127598458 | Common:3; Rare:73 | ||||
| chr3:128052196-128052526 | Common:2; Rare:110 | ||||
| chr3:128123727-128124026 | Rare:91 | ||||
| chr3:128153365-128153505 | Rare:41 | ||||
| chr3:128879408-128879675 | Common:4; Rare:129; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161006-129161433 | Common:2; Rare:135 | ||||
| chr3:129183810-129184091 | Common:2; Rare:98 | ||||
| chr3:129249531-129249680 | Common:1; Rare:47 | ||||
| chr3:129278664-129278895 | Common:4; Rare:67 | ||||
| chr3:129316283-129316511 | Common:1; Rare:54 | ||||
| chr3:129439847-129440325 | Common:1; Rare:143; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129560486-129560679 | Rare:46 | ||||
| chr3:129893574-129893891 | Rare:133 |