| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:443006-443323 | Common:11; Rare:127 | ||||
| chr5:612115-612391 | Rare:109 | ||||
| chr5:892396-892603 | Rare:56 | ||||
| chr5:892678-893029 | Common:5; Rare:126 | ||||
| chr5:1111997-1112169 | Rare:62 | ||||
| chr5:1295039-1295216 | Rare:52; Clinvar:1 | ||||
| chr5:1345021-1345297 | Common:2; Rare:100 | ||||
| chr5:1494824-1495105 | Common:1; Rare:91 | ||||
| chr5:1523861-1524420 | Common:3; Rare:168 | ||||
| chr5:1799272-1799480 | Common:2; Rare:53 | ||||
| chr5:1799761-1800000 | Common:8; Rare:112 | ||||
| chr5:1801254-1801474 | Common:4; Rare:115; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:5422060-5422778 | Common:3; Rare:234 | ||||
| chr5:6378036-6378247 | Common:2; Rare:42 | ||||
| chr5:6378426-6378777 | Rare:125 |