| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53891794-53892080 | Common:4; Rare:94 | ||||
| chr3:56557081-56557230 | Common:2; Rare:57 | ||||
| chr3:56682884-56682949 | Common:2; Rare:22 | ||||
| chr3:56683222-56683539 | Common:6; Rare:111 | ||||
| chr3:57079252-57079382 | Common:2; Rare:45 | ||||
| chr3:57227600-57227899 | Common:3; Rare:102 | ||||
| chr3:57555992-57556343 | Rare:91 | ||||
| chr3:57597295-57597800 | Common:7; Rare:151 | ||||
| chr3:57692979-57693178 | Common:1; Rare:58 | ||||
| chr3:58008312-58008439 | Common:1; Rare:46; Clinvar:1 | ||||
| chr3:58332800-58332964 | Common:3; Rare:46 | ||||
| chr3:58433805-58433952 | Rare:57; Clinvar (benign):2 | ||||
| chr3:59049905-59050159 | Rare:87 | ||||
| chr3:62318888-62319088 | Rare:86 | ||||
| chr3:63863743-63864158 | Common:8; Rare:138 |