| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57170221-57170384 | Common:2; Rare:42 | ||||
| chr3:57227526-57227938 | Common:12; Rare:383 | ||||
| chr3:57555876-57556368 | Common:2; Rare:353 | ||||
| chr3:57596446-57596728 | Common:4; Rare:91 | ||||
| chr3:57597233-57597846 | Common:22; Rare:511 | ||||
| chr3:57692591-57692724 | Common:1; Rare:34 | ||||
| chr3:57692680-57692862 | Common:2; Rare:60 | ||||
| chr3:57692939-57693264 | Common:4; Rare:241 | ||||
| chr3:57756239-57756363 | Rare:36 | ||||
| chr3:57756320-57756765 | Common:5; Rare:179 | ||||
| chr3:58008261-58008817 | Common:4; Rare:343; Clinvar:18; Clinvar (benign):4 | ||||
| chr3:58237290-58237650 | Common:14; Rare:141 | ||||
| chr3:58306126-58306370 | Common:2; Rare:126 | ||||
| chr3:58306429-58306635 | Common:6; Rare:137 | ||||
| chr3:58332540-58333090 | Common:13; Rare:162 |