| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138331777-138332128 | Common:2; Rare:84 | ||||
| chr5:138543104-138543496 | Common:2; Rare:116 | ||||
| chr5:138575650-138575798 | Rare:39 | ||||
| chr5:139198295-139198531 | Rare:78 | ||||
| chr5:139273975-139274142 | Rare:77 | ||||
| chr5:139293581-139293786 | Rare:68 | ||||
| chr5:139341769-139341933 | Common:1; Rare:46 | ||||
| chr5:139404046-139404270 | Rare:68 | ||||
| chr5:140175025-140175208 | Rare:50 | ||||
| chr5:140547541-140547679 | Common:1; Rare:27 | ||||
| chr5:140557419-140557519 | Rare:61 | ||||
| chr5:140564573-140564837 | Rare:73 | ||||
| chr5:140639275-140639478 | Common:3; Rare:50 | ||||
| chr5:140647576-140647890 | Common:5; Rare:129; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664747-140664907 | Common:2; Rare:40 |