| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:21176860-21177129 | Rare:74 | ||||
| chr1:21345474-21345655 | Common:1; Rare:70 | ||||
| chr1:21440047-21440179 | Common:1; Rare:29 | ||||
| chr1:21782955-21783277 | Common:2; Rare:115 | ||||
| chr1:22451731-22451879 | Common:1; Rare:54 | ||||
| chr1:23344217-23344546 | Common:2; Rare:112 | ||||
| chr1:23344651-23344859 | Common:1; Rare:72 | ||||
| chr1:23368854-23368986 | Common:1; Rare:46 | ||||
| chr1:23559409-23559671 | Common:2; Rare:114 | ||||
| chr1:23691738-23692058 | Common:4; Rare:120; Clinvar:2; Clinvar (benign):3 | ||||
| chr1:23778247-23778540 | Common:9; Rare:141 | ||||
| chr1:23791075-23791241 | Rare:49 | ||||
| chr1:23799534-23799705 | Rare:26 | ||||
| chr1:23800734-23800959 | Common:1; Rare:78 | ||||
| chr1:23825405-23825509 | Common:2; Rare:38; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |