| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138178610-138178724 | Rare:29 | ||||
| chr5:138178935-138179178 | Common:3; Rare:51 | ||||
| chr5:138331747-138332099 | Common:2; Rare:90 | ||||
| chr5:138543109-138543481 | Common:2; Rare:112 | ||||
| chr5:138753243-138753498 | Common:2; Rare:88 | ||||
| chr5:139273975-139274142 | Rare:77 | ||||
| chr5:139439453-139439646 | Common:2; Rare:52 | ||||
| chr5:139561115-139561582 | Common:1; Rare:192 | ||||
| chr5:139561746-139561794 | Rare:15 | ||||
| chr5:140303050-140303191 | Common:1; Rare:47 | ||||
| chr5:140557426-140557510 | Rare:46 | ||||
| chr5:140564556-140564846 | Rare:76 | ||||
| chr5:140647576-140647902 | Common:5; Rare:133; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664770-140664874 | Rare:22 | ||||
| chr5:140691305-140691644 | Common:1; Rare:120; Clinvar:9; Clinvar (benign):1 |