| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184734016-184734403 | Common:7; Rare:156 | ||||
| chr4:184825965-184826177 | Common:5; Rare:74 | ||||
| chr4:185143105-185143290 | Common:3; Rare:57; Clinvar (benign):3 | ||||
| chr4:185203925-185204098 | Common:1; Rare:59 | ||||
| chr4:185396581-185396845 | Rare:85 | ||||
| chr4:185425870-185426272 | Common:4; Rare:121 | ||||
| chr4:185471054-185471412 | Common:10; Rare:46 | ||||
| chr4:185471722-185471852 | Common:1; Rare:45 | ||||
| chr4:185811695-185811858 | Common:1; Rare:37 | ||||
| chr4:186191544-186191815 | Common:4; Rare:89; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:189940631-189940991 | Common:11; Rare:132 | ||||
| chr5:191253-191492 | Common:2; Rare:52 | ||||
| chr5:218123-218369 | Common:3; Rare:103; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:612180-612351 | Rare:69 | ||||
| chr5:892520-892990 | Common:5; Rare:150 |