| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:189940611-189940919 | Common:7; Rare:101 | ||||
| chr5:218097-218376 | Common:4; Rare:120; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:271396-271695 | Common:2; Rare:127 | ||||
| chr5:443074-443185 | Common:3; Rare:48 | ||||
| chr5:611567-611967 | Common:5; Rare:82 | ||||
| chr5:612191-612393 | Rare:87 | ||||
| chr5:693334-693564 | Common:5; Rare:63 | ||||
| chr5:849669-850069 | Common:6; Rare:149 | ||||
| chr5:892771-892927 | Common:1; Rare:58 | ||||
| chr5:1112008-1112146 | Rare:52 | ||||
| chr5:1294901-1295401 | Common:6; Rare:257; Clinvar:5; Clinvar (benign):6 | ||||
| chr5:1344990-1345290 | Common:2; Rare:115 | ||||
| chr5:1523810-1524150 | Common:2; Rare:108 | ||||
| chr5:1799776-1799993 | Common:8; Rare:101 | ||||
| chr5:1801285-1801465 | Common:4; Rare:90; Clinvar:3; Clinvar (benign):1 |