| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139198276-139198531 | Rare:83; Clinvar (benign):1 | ||||
| chr5:139273975-139274135 | Rare:75 | ||||
| chr5:139293532-139293809 | Rare:89 | ||||
| chr5:139403984-139404330 | Common:1; Rare:99 | ||||
| chr5:139439452-139439597 | Common:1; Rare:40 | ||||
| chr5:139482608-139482863 | Rare:37 | ||||
| chr5:139561078-139561408 | Common:1; Rare:130 | ||||
| chr5:139561727-139561820 | Rare:34 | ||||
| chr5:139648464-139648828 | Rare:103 | ||||
| chr5:140043268-140043389 | Rare:28 | ||||
| chr5:140107708-140107856 | Rare:50 | ||||
| chr5:140107992-140108195 | Rare:60 | ||||
| chr5:140175015-140175285 | Common:2; Rare:65 | ||||
| chr5:140303057-140303153 | Common:1; Rare:34 | ||||
| chr5:140346597-140346732 | Common:1; Rare:39 |