| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:147055926-147056091 | Common:2; Rare:27 | ||||
| chr5:147234839-147235144 | Common:2; Rare:84 | ||||
| chr5:148268520-148268830 | Common:1; Rare:52 | ||||
| chr5:148383723-148384044 | Rare:84 | ||||
| chr5:149141392-149141543 | Rare:43 | ||||
| chr5:149345307-149345607 | Common:1; Rare:114 | ||||
| chr5:149551335-149551656 | Rare:77 | ||||
| chr5:149960575-149960923 | Rare:116; Clinvar:7 | ||||
| chr5:150155617-150155921 | Common:1; Rare:87 | ||||
| chr5:150357464-150357749 | Rare:94; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:150412623-150412947 | Common:1; Rare:82 | ||||
| chr5:150449662-150449803 | Common:4; Rare:49 | ||||
| chr5:150485854-150485998 | Common:2; Rare:33 | ||||
| chr5:150486160-150486357 | Common:1; Rare:43 | ||||
| chr5:150640513-150640853 | Rare:64 |