| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139648689-139648966 | Rare:77 | ||||
| chr5:140647592-140647868 | Common:5; Rare:115; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691288-140691482 | Common:2; Rare:70; Clinvar:7; Clinvar (benign):1 | ||||
| chr5:141320759-141320920 | Common:1; Rare:53 | ||||
| chr5:141636849-141636982 | Common:1; Rare:45 | ||||
| chr5:142325011-142325218 | Rare:64 | ||||
| chr5:149345339-149345531 | Common:1; Rare:61 | ||||
| chr5:149551361-149551624 | Rare:63 | ||||
| chr5:154038877-154038989 | Common:1; Rare:37 | ||||
| chr5:159263201-159263320 | Common:1; Rare:38 | ||||
| chr5:172959365-172959440 | Rare:28 | ||||
| chr5:177022635-177022743 | Rare:39 | ||||
| chr5:177303672-177303827 | Common:4; Rare:71 | ||||
| chr5:177516893-177517012 | Common:2; Rare:60; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:179806836-179807107 | Common:3; Rare:95 |