| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1919481-1919780 | Common:10; Rare:178 | ||||
| chr1:2003679-2004079 | Common:9; Rare:153 | ||||
| chr1:2050105-2050597 | Common:7; Rare:491 | ||||
| chr1:2133380-2133700 | Common:5; Rare:158 | ||||
| chr1:2193603-2194310 | Common:2; Rare:509 | ||||
| chr1:2194640-2195440 | Common:2; Rare:578 | ||||
| chr1:2199194-2199660 | Common:4; Rare:393 | ||||
| chr1:2207090-2207490 | Common:2; Rare:121 | ||||
| chr1:2212340-2212700 | Common:2; Rare:147 | ||||
| chr1:2212640-2212806 | Common:1; Rare:43 | ||||
| chr1:2212710-2212961 | Common:12; Rare:163 | ||||
| chr1:2212980-2213490 | Common:4; Rare:169 | ||||
| chr1:2228920-2229528 | Common:4; Rare:253; Clinvar:14; Clinvar (benign):26; Clinvar (pathogenic):1 | ||||
| chr1:2391010-2391410 | Common:2; Rare:87 | ||||
| chr1:2391463-2391935 | Common:14; Rare:953 |