| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32817937-32818115 | Common:1; Rare:67 | ||||
| chr3:32818180-32818404 | Rare:88 | ||||
| chr3:33097078-33097285 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:33277295-33277505 | Common:2; Rare:60 | ||||
| chr3:33645454-33645538 | Rare:9 | ||||
| chr3:33718057-33718311 | Rare:93 | ||||
| chr3:33798489-33798701 | Common:2; Rare:78 | ||||
| chr3:33799031-33799363 | Common:1; Rare:89 | ||||
| chr3:36993064-36993612 | Common:2; Rare:192; Clinvar:39; Clinvar (benign):18; Clinvar (pathogenic):4 | ||||
| chr3:36993663-36993870 | Rare:84; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:37176054-37176406 | Common:1; Rare:99 | ||||
| chr3:37243146-37243419 | Common:1; Rare:70 | ||||
| chr3:37243627-37243781 | Common:2; Rare:69 | ||||
| chr3:37451828-37452150 | Common:2; Rare:82 | ||||
| chr3:37861718-37861981 | Common:1; Rare:56 |