| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57555979-57556366 | Rare:217 | ||||
| chr3:57597159-57597838 | Common:15; Rare:374 | ||||
| chr3:57692440-57692810 | Common:10; Rare:190 | ||||
| chr3:57692973-57693162 | Common:2; Rare:104 | ||||
| chr3:57755917-57756334 | Common:1; Rare:150 | ||||
| chr3:58237423-58237592 | Common:14; Rare:105 | ||||
| chr3:58306461-58306607 | Common:6; Rare:96 | ||||
| chr3:58332726-58332977 | Common:10; Rare:99 | ||||
| chr3:58433769-58433957 | Rare:145; Clinvar:4; Clinvar (benign):6 | ||||
| chr3:58491640-58492172 | Common:4; Rare:202 | ||||
| chr3:58537118-58537478 | Common:4; Rare:122 | ||||
| chr3:61251317-61251604 | Common:8; Rare:121 | ||||
| chr3:61560864-61561126 | Common:7; Rare:154 | ||||
| chr3:61561398-61561668 | Common:4; Rare:169 | ||||
| chr3:63863749-63864181 | Common:10; Rare:211 |