| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50628093-50628286 | Common:9; Rare:93; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783618-50783822 | Common:2; Rare:62 | ||||
| chr3:8501660-8501833 | Rare:60 | ||||
| chr3:9363007-9363099 | Rare:33 | ||||
| chr3:9792388-9792583 | Rare:53 | ||||
| chr3:9792732-9793127 | Common:3; Rare:135 | ||||
| chr3:10026328-10026470 | Rare:42 | ||||
| chr3:12287747-12287926 | Common:5; Rare:32 | ||||
| chr3:12663823-12663963 | Rare:39; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:14124713-14125144 | Common:4; Rare:126; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178559-14178857 | Common:2; Rare:157; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651486-14651783 | Rare:78 | ||||
| chr3:14947213-14947583 | Common:4; Rare:165 | ||||
| chr3:15206024-15206278 | Rare:95 | ||||
| chr3:15427495-15427616 | Rare:46 |