| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:145858886-145859380 | Rare:287 | ||||
| chr1:145859691-145859981 | Common:7; Rare:228 | ||||
| chr1:145885780-145886290 | Common:5; Rare:240 | ||||
| chr1:145918632-145919121 | Common:6; Rare:316; Clinvar:4 | ||||
| chr1:145926920-145927380 | Common:2; Rare:161; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:145927360-145927754 | Common:1; Rare:217; Clinvar (pathogenic):1 | ||||
| chr1:145958040-145958250 | Rare:46 | ||||
| chr1:145963037-145963437 | Common:3; Rare:74 | ||||
| chr1:145964374-145964931 | Rare:214 | ||||
| chr1:145994880-145996190 | Common:6; Rare:1033 | ||||
| chr1:145996434-145996939 | Common:6; Rare:476 | ||||
| chr1:146938017-146938789 | Common:4; Rare:302 | ||||
| chr1:147172064-147172907 | Common:7; Rare:563 | ||||
| chr1:147224680-147225080 | Common:5; Rare:115 | ||||
| chr1:147225174-147225375 | Common:1; Rare:39 |