| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185956277-185956377 | Rare:25 | ||||
| chr4:189940564-189940991 | Common:13; Rare:141 | ||||
| chr5:218093-218403 | Common:4; Rare:125; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr5:443095-443272 | Common:9; Rare:79 | ||||
| chr5:612189-612357 | Rare:68 | ||||
| chr5:892611-892923 | Common:5; Rare:102 | ||||
| chr5:1799777-1799988 | Common:8; Rare:99 | ||||
| chr5:1801300-1801455 | Common:4; Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6378492-6378666 | Rare:74 | ||||
| chr5:7851022-7851210 | Common:2; Rare:34 | ||||
| chr5:7868995-7869204 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr5:9546001-9546361 | Common:9; Rare:91 | ||||
| chr5:10249866-10250377 | Common:19; Rare:245; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353597-10353913 | Common:3; Rare:115 | ||||
| chr5:10441805-10441957 | Common:1; Rare:46 |