| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:149423454-149423572 | Common:1; Rare:23 | ||||
| chr5:149424094-149424365 | Common:2; Rare:60 | ||||
| chr5:149424706-149425163 | Common:2; Rare:83 | ||||
| chr5:149427368-149427737 | Common:4; Rare:58 | ||||
| chr5:149430228-149430662 | Common:4; Rare:100 | ||||
| chr5:149430717-149431229 | Common:3; Rare:97 | ||||
| chr5:150056121-150056255 | Common:1; Rare:43; Clinvar (pathogenic):1 | ||||
| chr5:150410786-150410804 | Rare:4 | ||||
| chr5:150585883-150586026 | Common:4; Rare:28 | ||||
| chr5:150778659-150778906 | Common:2; Rare:92 | ||||
| chr5:150780239-150780464 | Rare:35 | ||||
| chr5:150946505-150946621 | Rare:27 | ||||
| chr5:151022303-151022585 | Common:2; Rare:50 | ||||
| chr5:151028956-151029260 | Common:2; Rare:50 | ||||
| chr5:151038125-151038392 | Rare:32 |