| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1615122-1615546 | Common:4; Rare:167 | ||||
| chr1:1658898-1659051 | Common:2; Rare:65 | ||||
| chr1:1659074-1659271 | Common:2; Rare:76 | ||||
| chr1:1692525-1692578 | Common:2; Rare:11 | ||||
| chr1:1692998-1693189 | Common:1; Rare:30 | ||||
| chr1:1724267-1724504 | Common:4; Rare:88 | ||||
| chr1:1890380-1890494 | Common:2; Rare:36 | ||||
| chr1:1890823-1891180 | Rare:126 | ||||
| chr1:2050203-2050510 | Common:2; Rare:121 | ||||
| chr1:2193643-2194353 | Common:2; Rare:253 | ||||
| chr1:2391470-2391955 | Common:2; Rare:169 | ||||
| chr1:2412492-2412776 | Common:2; Rare:122; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr1:3624747-3625052 | Common:1; Rare:103 | ||||
| chr1:3772414-3772800 | Common:3; Rare:91 | ||||
| chr1:3796471-3796628 | Common:2; Rare:55 |