| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140664673-140664904 | Common:4; Rare:52 | ||||
| chr5:140691300-140691620 | Common:1; Rare:117; Clinvar:10; Clinvar (benign):1 | ||||
| chr5:141320742-141320928 | Common:2; Rare:64 | ||||
| chr5:141636810-141637001 | Common:2; Rare:83 | ||||
| chr5:141923741-141923933 | Common:1; Rare:58 | ||||
| chr5:142324979-142325296 | Rare:104 | ||||
| chr5:143402969-143403139 | Common:1; Rare:38 | ||||
| chr5:144170572-144170873 | Common:2; Rare:99 | ||||
| chr5:146182501-146182936 | Common:4; Rare:130 | ||||
| chr5:148383722-148384018 | Rare:77 | ||||
| chr5:149141400-149141851 | Common:1; Rare:110 | ||||
| chr5:149551334-149551625 | Rare:68 | ||||
| chr5:150155718-150156038 | Rare:97 | ||||
| chr5:150245263-150245675 | Common:3; Rare:78 | ||||
| chr5:150449676-150449795 | Common:4; Rare:42 |