| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:56516986-56517127 | Common:1; Rare:22 | ||||
| chr1:56579219-56579511 | Common:3; Rare:65 | ||||
| chr1:56579528-56579601 | Rare:16 | ||||
| chr1:56579609-56579765 | Common:2; Rare:22 | ||||
| chr1:56645110-56645431 | Common:1; Rare:105 | ||||
| chr1:56818831-56819065 | Common:2; Rare:58 | ||||
| chr1:58546193-58546423 | Common:4; Rare:53 | ||||
| chr1:58546579-58546970 | Common:4; Rare:122 | ||||
| chr1:58577167-58577418 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:58577432-58577579 | Rare:30; Clinvar:1 | ||||
| chr1:58699973-58700203 | Common:4; Rare:105 | ||||
| chr1:58783960-58784468 | Common:2; Rare:134 | ||||
| chr1:58784574-58784802 | Common:3; Rare:61 | ||||
| chr1:59296448-59297157 | Common:15; Rare:194 | ||||
| chr1:59814435-59815096 | Common:8; Rare:184 |