| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:163437316-163437618 | Rare:89 | ||||
| chr5:163460372-163460664 | Common:5; Rare:61 | ||||
| chr5:163505440-163505667 | Common:1; Rare:75 | ||||
| chr5:168529223-168529369 | Common:3; Rare:34 | ||||
| chr5:168844810-168845109 | Common:1; Rare:57 | ||||
| chr5:169583609-169583889 | Common:7; Rare:83 | ||||
| chr5:171387514-171388006 | Rare:233; Clinvar:1 | ||||
| chr5:172454349-172454652 | Common:10; Rare:80; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172771180-172771432 | Common:4; Rare:108 | ||||
| chr5:172834163-172834416 | Common:1; Rare:61 | ||||
| chr5:172959370-172959507 | Common:1; Rare:48 | ||||
| chr5:173056148-173056415 | Common:1; Rare:74 | ||||
| chr5:173328416-173328596 | Rare:34 | ||||
| chr5:173889842-173890181 | Rare:82 | ||||
| chr5:173890510-173890568 | Rare:9 |