| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161038879-161039072 | Common:2; Rare:61 | ||||
| chr1:161039113-161039289 | Common:1; Rare:27 | ||||
| chr1:161044961-161045089 | Rare:28 | ||||
| chr1:161045866-161046064 | Common:1; Rare:51 | ||||
| chr1:161069822-161070124 | Rare:39 | ||||
| chr1:161117951-161118129 | Rare:80 | ||||
| chr1:161132432-161132637 | Common:1; Rare:72 | ||||
| chr1:161153782-161154073 | Common:1; Rare:85; Clinvar (pathogenic):1 | ||||
| chr1:161159404-161159507 | Common:1; Rare:26 | ||||
| chr1:161166268-161166528 | Common:2; Rare:62; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:161168820-161169124 | Rare:87; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr1:161176223-161176426 | Rare:35 | ||||
| chr1:161209706-161209887 | Rare:40; Clinvar (benign):1 | ||||
| chr1:161306178-161306415 | Rare:84; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:161314302-161314405 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):2 |