| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:925600-925721 | Common:1; Rare:39 | ||||
| chr1:1324580-1324938 | Common:3; Rare:167 | ||||
| chr1:1353853-1354129 | Common:1; Rare:137; Clinvar (pathogenic):1 | ||||
| chr1:1358512-1358750 | Common:1; Rare:85 | ||||
| chr1:1390265-1390561 | Rare:92 | ||||
| chr1:1399214-1399575 | Common:1; Rare:166 | ||||
| chr1:1407186-1407420 | Common:1; Rare:106 | ||||
| chr1:1615350-1615546 | Common:2; Rare:95 | ||||
| chr1:1615773-1616023 | Common:1; Rare:70 | ||||
| chr1:1631359-1631714 | Common:5; Rare:108 | ||||
| chr1:1632014-1632175 | Common:2; Rare:54 | ||||
| chr1:1658926-1659046 | Common:2; Rare:45 | ||||
| chr1:1692455-1692544 | Common:2; Rare:12 | ||||
| chr1:1724242-1724466 | Common:3; Rare:78 | ||||
| chr1:1780004-1780223 | Rare:48 |