| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185396581-185396655 | Rare:18 | ||||
| chr4:185425901-185426267 | Common:3; Rare:105 | ||||
| chr4:185535493-185535766 | Common:2; Rare:64 | ||||
| chr4:186250338-186250543 | Rare:55 | ||||
| chr4:186723707-186723890 | Common:4; Rare:76 | ||||
| chr4:188109327-188109355 | Rare:8 | ||||
| chr4:188109359-188109417 | Rare:16 | ||||
| chr4:189940593-189940969 | Common:11; Rare:126 | ||||
| chr5:218134-218361 | Common:3; Rare:90; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:443095-443246 | Common:5; Rare:67 | ||||
| chr5:892529-892990 | Common:5; Rare:145 | ||||
| chr5:1523826-1524106 | Rare:91 | ||||
| chr5:1799790-1799993 | Common:5; Rare:95 | ||||
| chr5:1801287-1801480 | Common:4; Rare:100; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:5140096-5140320 | Common:5; Rare:65 |