| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:189940620-189940968 | Common:9; Rare:123 | ||||
| chr5:218112-218361 | Common:3; Rare:100; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:612211-612346 | Rare:51 | ||||
| chr5:892625-892917 | Common:5; Rare:96 | ||||
| chr5:1799785-1799949 | Common:7; Rare:83 | ||||
| chr5:1801309-1801455 | Common:4; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422325-5422677 | Common:2; Rare:115 | ||||
| chr5:6378485-6378666 | Rare:78 | ||||
| chr5:7869000-7869196 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr5:10249856-10250160 | Common:16; Rare:148 | ||||
| chr5:10353590-10353925 | Common:3; Rare:122 | ||||
| chr5:11903239-11903477 | Rare:48 | ||||
| chr5:16465715-16465894 | Rare:32 | ||||
| chr5:16713433-16713585 | Rare:40 | ||||
| chr5:17216220-17216546 | Rare:68 |