| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46335595-46335769 | Common:2; Rare:76; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:46762496-46762707 | Common:3; Rare:80 | ||||
| chr22:50185704-50185938 | Common:4; Rare:96 | ||||
| chr22:50628082-50628286 | Common:9; Rare:100; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783585-50783859 | Common:2; Rare:91 | ||||
| chr3:3126813-3126990 | Common:4; Rare:78; Clinvar (benign):2 | ||||
| chr3:4303253-4303411 | Common:1; Rare:61 | ||||
| chr3:4493165-4493350 | Rare:66 | ||||
| chr3:4979182-4979606 | Common:2; Rare:94 | ||||
| chr3:5187354-5187663 | Common:5; Rare:126 | ||||
| chr3:8501649-8501947 | Common:2; Rare:108 | ||||
| chr3:9362950-9363127 | Common:2; Rare:64 | ||||
| chr3:9397822-9397891 | Rare:13 | ||||
| chr3:9749755-9750007 | Rare:84 | ||||
| chr3:9792382-9792570 | Rare:52 |