| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:21345463-21345677 | Common:2; Rare:82 | ||||
| chr1:21622549-21622711 | Common:3; Rare:53 | ||||
| chr1:21782977-21783182 | Common:1; Rare:69 | ||||
| chr1:23019277-23019635 | Rare:126 | ||||
| chr1:23019809-23019821 | Rare:1 | ||||
| chr1:23077001-23077353 | Common:1; Rare:71 | ||||
| chr1:23194795-23194965 | Common:1; Rare:39 | ||||
| chr1:23344180-23344438 | Common:2; Rare:99 | ||||
| chr1:23368161-23368494 | Common:1; Rare:100 | ||||
| chr1:23368883-23369241 | Common:3; Rare:103 | ||||
| chr1:23558909-23559159 | Common:5; Rare:126 | ||||
| chr1:23559311-23559648 | Common:1; Rare:148 | ||||
| chr1:23778238-23778451 | Common:6; Rare:109 | ||||
| chr1:23799516-23799793 | Rare:50 | ||||
| chr1:23825401-23825725 | Common:3; Rare:77; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |