| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123585525-123585613 | Rare:16 | ||||
| chr3:125375236-125375358 | Rare:35 | ||||
| chr3:125595522-125595739 | Rare:69 | ||||
| chr3:126084099-126084219 | Common:1; Rare:51 | ||||
| chr3:127598258-127598428 | Common:2; Rare:42 | ||||
| chr3:127823112-127823167 | Rare:16 | ||||
| chr3:128052137-128052532 | Common:4; Rare:134 | ||||
| chr3:128153365-128153496 | Rare:37 | ||||
| chr3:128726140-128726225 | Common:1; Rare:31; Clinvar:3 | ||||
| chr3:128879421-128879704 | Common:4; Rare:139; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129183774-129184045 | Common:2; Rare:86 | ||||
| chr3:129249552-129249686 | Common:1; Rare:41 | ||||
| chr3:129315868-129316094 | Common:2; Rare:55 | ||||
| chr3:129316279-129316361 | Common:1; Rare:28 | ||||
| chr3:129439847-129440158 | Common:1; Rare:97; Clinvar:1; Clinvar (benign):1 |