| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:233613390-233613826 | Common:4; Rare:137 | ||||
| chr1:233613760-233614221 | Common:10; Rare:266 | ||||
| chr1:233614327-233614730 | Common:3; Rare:151 | ||||
| chr1:234214030-234214310 | Rare:58 | ||||
| chr1:234373207-234373841 | Common:5; Rare:593; Clinvar (benign):21 | ||||
| chr1:234478500-234478686 | Common:4; Rare:109 | ||||
| chr1:234478780-234479030 | Common:5; Rare:123 | ||||
| chr1:234479069-234479287 | Common:16; Rare:193 | ||||
| chr1:234608041-234608543 | Common:7; Rare:448; Clinvar (benign):2 | ||||
| chr1:235128689-235129123 | Common:2; Rare:429 | ||||
| chr1:235129261-235129521 | Rare:59 | ||||
| chr1:235160606-235160886 | Common:3; Rare:78 | ||||
| chr1:235160865-235161601 | Common:9; Rare:783 | ||||
| chr1:235325945-235327000 | Common:7; Rare:294 | ||||
| chr1:235328079-235329087 | Common:15; Rare:738 |