| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:124730376-124730474 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:125375135-125375426 | Rare:83 | ||||
| chr3:125595538-125595605 | Rare:28 | ||||
| chr3:126084103-126084223 | Common:1; Rare:53 | ||||
| chr3:127598265-127598440 | Common:2; Rare:42 | ||||
| chr3:127628965-127629211 | Common:1; Rare:82 | ||||
| chr3:127672808-127673014 | Common:3; Rare:99 | ||||
| chr3:128052202-128052532 | Common:2; Rare:111 | ||||
| chr3:128153365-128153510 | Rare:45 | ||||
| chr3:128879425-128879694 | Common:4; Rare:135; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129160998-129161133 | Rare:55 | ||||
| chr3:129183783-129184081 | Common:2; Rare:101 | ||||
| chr3:129249509-129249683 | Common:3; Rare:53 | ||||
| chr3:129278761-129278895 | Common:4; Rare:43 | ||||
| chr3:129316272-129316383 | Common:1; Rare:37 |