| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140691262-140691639 | Common:2; Rare:134; Clinvar:10; Clinvar (benign):2 | ||||
| chr5:141320722-141320928 | Common:3; Rare:71 | ||||
| chr5:141636803-141637011 | Common:2; Rare:93 | ||||
| chr5:142324992-142325236 | Rare:78 | ||||
| chr5:146203422-146203662 | Common:2; Rare:78 | ||||
| chr5:148383870-148384029 | Rare:51 | ||||
| chr5:149141666-149141845 | Common:1; Rare:35 | ||||
| chr5:149345339-149345537 | Common:1; Rare:66 | ||||
| chr5:149357825-149358057 | Common:6; Rare:55 | ||||
| chr5:149551353-149551625 | Rare:64 | ||||
| chr5:150485852-150485978 | Common:2; Rare:30 | ||||
| chr5:150486184-150486348 | Common:1; Rare:34 | ||||
| chr5:151771396-151771739 | Common:1; Rare:110 | ||||
| chr5:151771747-151772023 | Common:3; Rare:100 | ||||
| chr5:154038882-154039006 | Common:1; Rare:41 |