| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:41201485-41201596 | Common:1; Rare:24 | ||||
| chr3:41221281-41221342 | Rare:14 | ||||
| chr3:41233125-41233401 | Common:1; Rare:47 | ||||
| chr3:41237744-41238046 | Common:1; Rare:74 | ||||
| chr3:43347202-43347385 | Rare:47 | ||||
| chr3:43366879-43367156 | Common:1; Rare:74 | ||||
| chr3:45093581-45093728 | Rare:38 | ||||
| chr3:46989079-46989331 | Rare:82; Clinvar:1 | ||||
| chr3:47164775-47164818 | Common:1; Rare:13 | ||||
| chr3:48691745-48691974 | Common:3; Rare:46 | ||||
| chr3:49101429-49101640 | Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:49680941-49681167 | Rare:43 | ||||
| chr3:49897321-49897675 | Rare:123 | ||||
| chr3:49998350-49998420 | Rare:9 | ||||
| chr3:50358428-50358606 | Rare:59 |