| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53891793-53892088 | Common:5; Rare:98 | ||||
| chr3:56557042-56557239 | Common:2; Rare:89 | ||||
| chr3:56682947-56683406 | Common:4; Rare:158 | ||||
| chr3:57079269-57079382 | Common:2; Rare:40 | ||||
| chr3:57227600-57227922 | Common:4; Rare:107 | ||||
| chr3:57555996-57556325 | Rare:82 | ||||
| chr3:57597286-57597839 | Common:7; Rare:168 | ||||
| chr3:57692966-57693198 | Common:1; Rare:69 | ||||
| chr3:57756155-57756322 | Rare:41 | ||||
| chr3:58008312-58008600 | Common:1; Rare:104; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:58433794-58434059 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:59049972-59050163 | Rare:65 | ||||
| chr3:61251370-61251597 | Common:4; Rare:55 | ||||
| chr3:61561439-61561587 | Common:1; Rare:50 | ||||
| chr3:62318875-62319115 | Rare:97 |