| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123692335-123692402 | Rare:16 | ||||
| chr3:123700936-123701284 | Rare:74; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:123701436-123701642 | Common:1; Rare:66; Clinvar:7 | ||||
| chr3:125375218-125375391 | Rare:46 | ||||
| chr3:125595258-125595403 | Common:2; Rare:44 | ||||
| chr3:125595489-125595636 | Common:1; Rare:50 | ||||
| chr3:126083990-126084219 | Common:2; Rare:79 | ||||
| chr3:127590691-127590912 | Common:2; Rare:48 | ||||
| chr3:127598248-127598472 | Common:2; Rare:69 | ||||
| chr3:127672796-127673028 | Common:4; Rare:115 | ||||
| chr3:127822455-127822475 | Rare:3 | ||||
| chr3:127822477-127822552 | Rare:17 | ||||
| chr3:128052149-128052532 | Common:3; Rare:128 | ||||
| chr3:128064605-128064903 | Common:2; Rare:61 | ||||
| chr3:128067219-128067593 | Rare:91 |