| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145098156-145098348 | Rare:69 | ||||
| chr4:152779721-152779993 | Common:1; Rare:74 | ||||
| chr4:158671853-158672127 | Common:4; Rare:68 | ||||
| chr4:174283664-174283904 | Common:1; Rare:43 | ||||
| chr4:177442376-177442519 | Rare:86; Clinvar:2 | ||||
| chr4:183659122-183659335 | Common:1; Rare:65 | ||||
| chr4:184474512-184474816 | Rare:66 | ||||
| chr4:184649442-184649786 | Common:4; Rare:110 | ||||
| chr4:185425944-185426009 | Rare:23 | ||||
| chr5:218112-218369 | Common:3; Rare:107; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:892730-892923 | Common:2; Rare:75 | ||||
| chr5:1799790-1799956 | Common:5; Rare:81 | ||||
| chr5:1801346-1801455 | Common:1; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:10249874-10250361 | Common:19; Rare:236; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353597-10353896 | Common:3; Rare:108 |