| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:158284073-158284473 | Common:1; Rare:109 | ||||
| chr1:158285710-158286230 | Common:6; Rare:134 | ||||
| chr1:158286670-158287351 | Common:3; Rare:181 | ||||
| chr1:158830090-158830340 | Rare:42 | ||||
| chr1:158952000-158952260 | Common:4; Rare:67 | ||||
| chr1:159010527-159010737 | Rare:40 | ||||
| chr1:159012495-159012981 | Common:4; Rare:270 | ||||
| chr1:159041155-159041555 | Common:2; Rare:75 | ||||
| chr1:159068101-159068526 | Rare:111 | ||||
| chr1:159187835-159189532 | Common:6; Rare:515 | ||||
| chr1:159890074-159890186 | Rare:32 | ||||
| chr1:159910506-159910753 | Rare:78 | ||||
| chr1:159921180-159921440 | Common:4; Rare:72 | ||||
| chr1:159922146-159922546 | Common:4; Rare:210 | ||||
| chr1:160030810-160031060 | Rare:84; Clinvar (benign):1 |