| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:160356263-160356417 | Rare:35 | ||||
| chr1:160739133-160739326 | Common:1; Rare:57 | ||||
| chr1:161020716-161020982 | Rare:67 | ||||
| chr1:161021078-161021533 | Common:6; Rare:121 | ||||
| chr1:161038880-161039263 | Common:3; Rare:90 | ||||
| chr1:161045855-161046057 | Common:1; Rare:52 | ||||
| chr1:161117952-161118182 | Rare:116 | ||||
| chr1:161118188-161118382 | Common:1; Rare:55 | ||||
| chr1:161132365-161132703 | Common:1; Rare:106 | ||||
| chr1:161153716-161153887 | Common:1; Rare:36 | ||||
| chr1:161166228-161166578 | Common:4; Rare:91; Clinvar:5; Clinvar (benign):2 | ||||
| chr1:161199049-161199284 | Rare:38 | ||||
| chr1:161209478-161209929 | Common:1; Rare:99; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr1:161225765-161226090 | Common:10; Rare:47 | ||||
| chr1:161314269-161314422 | Common:3; Rare:62; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 |