| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:154038871-154039010 | Common:1; Rare:49 | ||||
| chr5:154850574-154850738 | Common:1; Rare:31 | ||||
| chr5:154857767-154857889 | Rare:33 | ||||
| chr5:154858414-154858722 | Common:1; Rare:99 | ||||
| chr5:154941007-154941112 | Common:1; Rare:45 | ||||
| chr5:159263201-159263337 | Common:1; Rare:45 | ||||
| chr5:160419049-160419242 | Common:3; Rare:72 | ||||
| chr5:163460376-163460657 | Common:5; Rare:60 | ||||
| chr5:163505438-163505684 | Common:1; Rare:82 | ||||
| chr5:172188163-172188510 | Common:1; Rare:93 | ||||
| chr5:172454327-172454655 | Common:10; Rare:92; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172771184-172771470 | Common:4; Rare:115 | ||||
| chr5:172834163-172834430 | Common:1; Rare:65 | ||||
| chr5:172958791-172958925 | Common:2; Rare:41 | ||||
| chr5:172959390-172959497 | Common:1; Rare:38 |