| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184649406-184649775 | Common:4; Rare:122 | ||||
| chr4:184734038-184734377 | Common:5; Rare:135 | ||||
| chr4:185396581-185396843 | Rare:83 | ||||
| chr4:185425872-185426272 | Common:4; Rare:120 | ||||
| chr4:186723787-186723936 | Common:4; Rare:57 | ||||
| chr4:189940605-189941012 | Common:16; Rare:144 | ||||
| chr5:218117-218396 | Common:3; Rare:117; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr5:443069-443269 | Common:10; Rare:90 | ||||
| chr5:612191-612351 | Rare:64 | ||||
| chr5:892631-892941 | Common:5; Rare:104 | ||||
| chr5:1799782-1799988 | Common:8; Rare:96 | ||||
| chr5:1801300-1801473 | Common:4; Rare:90; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:5422334-5422646 | Common:2; Rare:97 | ||||
| chr5:6378498-6378675 | Rare:69 | ||||
| chr5:7869000-7869204 | Common:2; Rare:103; Clinvar (benign):1 |