| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46250268-46250404 | Common:1; Rare:43 | ||||
| chr22:46267832-46268037 | Common:1; Rare:62 | ||||
| chr22:46335601-46335797 | Common:5; Rare:91; Clinvar:9; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762496-46762701 | Common:3; Rare:76 | ||||
| chr22:50185690-50185949 | Common:4; Rare:109 | ||||
| chr22:50244960-50245059 | Common:2; Rare:39 | ||||
| chr22:50628087-50628272 | Common:9; Rare:89; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783585-50783859 | Common:2; Rare:91 | ||||
| chr3:3126773-3127005 | Common:4; Rare:105; Clinvar (benign):3 | ||||
| chr3:3128762-3129057 | Common:2; Rare:75; Clinvar (benign):1 | ||||
| chr3:4303124-4303424 | Common:2; Rare:92 | ||||
| chr3:4493156-4493503 | Common:1; Rare:117; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4812922-4813201 | Rare:72; Clinvar (benign):2 | ||||
| chr3:8501532-8501964 | Common:3; Rare:158 | ||||
| chr3:9362948-9363098 | Common:2; Rare:54 |