| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:189940655-189941012 | Common:14; Rare:131 | ||||
| chr5:168443-168629 | Common:2; Rare:45 | ||||
| chr5:218109-218352 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:271291-271383 | Common:1; Rare:16 | ||||
| chr5:443061-443288 | Common:10; Rare:104 | ||||
| chr5:612191-612364 | Rare:69 | ||||
| chr5:892440-893087 | Common:5; Rare:205 | ||||
| chr5:1799770-1799993 | Common:8; Rare:105 | ||||
| chr5:1801283-1801531 | Common:4; Rare:128; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:5422342-5422731 | Common:2; Rare:129 | ||||
| chr5:6378116-6378536 | Common:1; Rare:128 | ||||
| chr5:6378540-6378733 | Rare:65 | ||||
| chr5:6621788-6622041 | Common:3; Rare:72; Clinvar (benign):2 | ||||
| chr5:6632879-6633460 | Common:11; Rare:191; Clinvar:10; Clinvar (benign):7 | ||||
| chr5:7868977-7869243 | Common:2; Rare:141; Clinvar:2; Clinvar (benign):3 |