| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50783628-50783882 | Common:1; Rare:74 | ||||
| chr3:197125-197332 | Common:1; Rare:68 | ||||
| chr3:2098616-2098962 | Common:4; Rare:137 | ||||
| chr3:3126813-3126975 | Common:4; Rare:70; Clinvar (benign):1 | ||||
| chr3:4493151-4493350 | Common:1; Rare:70 | ||||
| chr3:8501641-8501941 | Common:2; Rare:110 | ||||
| chr3:9249627-9249750 | Common:1; Rare:34 | ||||
| chr3:9363020-9363108 | Rare:31 | ||||
| chr3:9397436-9397717 | Common:1; Rare:102 | ||||
| chr3:9749732-9750010 | Common:1; Rare:94 | ||||
| chr3:9792414-9792570 | Rare:40 | ||||
| chr3:9916952-9917147 | Common:2; Rare:42 | ||||
| chr3:9933507-9933879 | Common:2; Rare:150; Clinvar:3 | ||||
| chr3:10026334-10026473 | Rare:39 | ||||
| chr3:11719453-11719579 | Rare:37 |