| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:125595258-125595353 | Common:2; Rare:35 | ||||
| chr3:125595498-125595746 | Common:2; Rare:77 | ||||
| chr3:126084103-126084200 | Common:1; Rare:36 | ||||
| chr3:126180023-126180077 | Rare:12 | ||||
| chr3:126180482-126180666 | Rare:37 | ||||
| chr3:126704081-126704284 | Common:2; Rare:59 | ||||
| chr3:127672808-127673028 | Common:4; Rare:106 | ||||
| chr3:128052194-128052504 | Common:2; Rare:100 | ||||
| chr3:128153356-128153502 | Rare:40 | ||||
| chr3:128493193-128493267 | Rare:25 | ||||
| chr3:128879421-128879671 | Common:4; Rare:122; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129001232-129001355 | Common:1; Rare:32 | ||||
| chr3:129160995-129161116 | Rare:47 | ||||
| chr3:129183777-129184045 | Common:2; Rare:86 | ||||
| chr3:129249273-129249724 | Common:4; Rare:129 |