| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:31532394-31532665 | Common:4; Rare:78 | ||||
| chr3:31533038-31533293 | Common:1; Rare:80; Clinvar (benign):2 | ||||
| chr3:32106404-32106720 | Common:4; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570636-32570962 | Common:1; Rare:144 | ||||
| chr3:33097094-33097267 | Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33114387-33114548 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:33277289-33277482 | Common:2; Rare:52 | ||||
| chr3:33718050-33718308 | Rare:98 | ||||
| chr3:33798374-33798686 | Common:2; Rare:95 | ||||
| chr3:33798985-33799070 | Rare:30 | ||||
| chr3:36993080-36993569 | Common:2; Rare:167; Clinvar:28; Clinvar (benign):13; Clinvar (pathogenic):3 | ||||
| chr3:37176105-37176410 | Common:1; Rare:83 | ||||
| chr3:37243200-37243388 | Common:1; Rare:47 | ||||
| chr3:37861719-37861862 | Rare:36 | ||||
| chr3:38024510-38024667 | Common:1; Rare:59 |