| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52535011-52535100 | Common:1; Rare:17 | ||||
| chr3:52536330-52536762 | Common:3; Rare:139 | ||||
| chr3:52685544-52685839 | Common:2; Rare:76 | ||||
| chr3:52685937-52686105 | Common:2; Rare:71 | ||||
| chr3:52693089-52693295 | Common:1; Rare:70 | ||||
| chr3:52695986-52696157 | Common:1; Rare:38 | ||||
| chr3:52705548-52706327 | Common:5; Rare:251 | ||||
| chr3:52770805-52771044 | Common:5; Rare:59 | ||||
| chr3:52799015-52799176 | Rare:37 | ||||
| chr3:52823661-52823841 | Common:1; Rare:46 | ||||
| chr3:53130378-53130545 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53161121-53161385 | Common:3; Rare:64 | ||||
| chr3:53255959-53256115 | Common:1; Rare:72 | ||||
| chr3:53347494-53347734 | Common:2; Rare:79 | ||||
| chr3:53846152-53846377 | Common:2; Rare:54 |