| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53347504-53347763 | Common:2; Rare:86 | ||||
| chr3:53844929-53844972 | Rare:8 | ||||
| chr3:53846335-53846585 | Common:1; Rare:80 | ||||
| chr3:53891794-53892075 | Common:4; Rare:94 | ||||
| chr3:56557081-56557238 | Common:2; Rare:61 | ||||
| chr3:57227615-57227913 | Common:3; Rare:103 | ||||
| chr3:57555996-57556339 | Rare:87 | ||||
| chr3:57597277-57597737 | Common:4; Rare:141 | ||||
| chr3:57693036-57693170 | Common:1; Rare:36 | ||||
| chr3:58211180-58211234 | Rare:9 | ||||
| chr3:58433769-58434058 | Common:2; Rare:109; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:58491793-58492159 | Common:3; Rare:92 | ||||
| chr3:58537118-58537270 | Common:1; Rare:32 | ||||
| chr3:59049884-59050103 | Rare:74 | ||||
| chr3:61251308-61251597 | Common:4; Rare:71 |