| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:153633884-153634123 | Common:4; Rare:74 | ||||
| chr1:153670918-153671177 | Rare:77 | ||||
| chr1:153727746-153728092 | Common:1; Rare:103 | ||||
| chr1:153963477-153963745 | Common:2; Rare:73 | ||||
| chr1:153967301-153967515 | Common:1; Rare:45 | ||||
| chr1:153967619-153967942 | Common:1; Rare:57 | ||||
| chr1:153986241-153986435 | Rare:49 | ||||
| chr1:153990490-153990814 | Common:2; Rare:106 | ||||
| chr1:154220534-154220984 | Common:1; Rare:149 | ||||
| chr1:154272411-154272682 | Common:4; Rare:62; Clinvar:1; Clinvar (benign):3 | ||||
| chr1:154627890-154628039 | Common:3; Rare:78 | ||||
| chr1:154936672-154936762 | Common:2; Rare:29 | ||||
| chr1:154956085-154956287 | Common:1; Rare:60 | ||||
| chr1:154961712-154962050 | Common:1; Rare:116 | ||||
| chr1:154970729-154970844 | Rare:22 |