| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48440066-48440303 | Common:1; Rare:89 | ||||
| chr3:48918804-48918865 | Common:2; Rare:33 | ||||
| chr3:49104750-49104894 | Rare:53; Clinvar (benign):3 | ||||
| chr3:49411909-49412213 | Common:1; Rare:108 | ||||
| chr3:51385012-51385347 | Common:2; Rare:102 | ||||
| chr3:52685813-52686072 | Common:2; Rare:101 | ||||
| chr3:52705789-52706216 | Common:2; Rare:149 | ||||
| chr3:53891802-53892056 | Common:2; Rare:84 | ||||
| chr3:57597319-57597737 | Common:4; Rare:126 | ||||
| chr3:58433810-58434082 | Common:2; Rare:89; Clinvar (benign):2 | ||||
| chr3:62318932-62319049 | Rare:46 | ||||
| chr3:67654592-67654795 | Common:2; Rare:75 | ||||
| chr3:81761642-81761765 | Common:1; Rare:43; Clinvar:1 | ||||
| chr3:88058967-88059261 | Common:2; Rare:90 | ||||
| chr3:100492413-100492626 | Common:2; Rare:73 |