| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:230978886-230979106 | Rare:79 | ||||
| chr1:231241122-231241333 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:231337819-231338056 | Common:2; Rare:86 | ||||
| chr1:231528495-231528738 | Common:2; Rare:82 | ||||
| chr1:234373387-234373539 | Common:1; Rare:78; Clinvar (benign):3 | ||||
| chr1:234373645-234373768 | Rare:49; Clinvar (benign):3 | ||||
| chr1:234608177-234608246 | Rare:22 | ||||
| chr1:235866847-235867142 | Common:3; Rare:87 | ||||
| chr1:236064966-236065333 | Common:3; Rare:133; Clinvar (pathogenic):1 | ||||
| chr1:236281936-236282063 | Common:2; Rare:34 | ||||
| chr1:236518040-236518281 | Rare:51 | ||||
| chr1:236523845-236524034 | Common:2; Rare:51 | ||||
| chr1:243255046-243255358 | Common:1; Rare:70 | ||||
| chr1:243255448-243255490 | Rare:7 | ||||
| chr1:243255776-243256140 | Common:1; Rare:107; Clinvar:4; Clinvar (benign):1 |