| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52685937-52686171 | Common:2; Rare:93 | ||||
| chr3:52705558-52706227 | Common:4; Rare:213 | ||||
| chr3:52770921-52771025 | Common:2; Rare:24 | ||||
| chr3:53130384-53130523 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53255959-53256180 | Common:2; Rare:96 | ||||
| chr3:53347504-53347734 | Common:2; Rare:74 | ||||
| chr3:53891794-53892054 | Common:2; Rare:83 | ||||
| chr3:56557055-56557245 | Common:2; Rare:83 | ||||
| chr3:57079252-57079388 | Common:2; Rare:45 | ||||
| chr3:57227636-57227931 | Common:4; Rare:91 | ||||
| chr3:57292656-57293065 | Common:3; Rare:67 | ||||
| chr3:57555996-57556321 | Rare:81 | ||||
| chr3:57597330-57597785 | Common:5; Rare:135 | ||||
| chr3:57693025-57693172 | Common:1; Rare:47 | ||||
| chr3:57889885-57890099 | Rare:48; Clinvar (benign):2 |