| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:159712334-159712641 | Common:2; Rare:107 | ||||
| chr2:160062501-160062743 | Common:5; Rare:58 | ||||
| chr2:160271231-160271447 | Rare:45 | ||||
| chr2:160493378-160493595 | Common:1; Rare:72 | ||||
| chr2:160493794-160494051 | Common:1; Rare:59 | ||||
| chr2:161308334-161308537 | Common:2; Rare:53 | ||||
| chr2:162073975-162074296 | Common:1; Rare:87 | ||||
| chr2:162318483-162318804 | Common:2; Rare:63 | ||||
| chr2:162838714-162838771 | Rare:17 | ||||
| chr2:163735852-163736107 | Common:2; Rare:43 | ||||
| chr2:164840542-164840760 | Common:1; Rare:39 | ||||
| chr2:164841192-164841350 | Rare:48 | ||||
| chr2:164841783-164841926 | Common:1; Rare:40 | ||||
| chr2:164955442-164955658 | Rare:52 | ||||
| chr2:165953718-165953847 | Rare:66; Clinvar:9; Clinvar (benign):1 |