| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138753236-138753507 | Common:2; Rare:92 | ||||
| chr5:139198284-139198567 | Rare:97; Clinvar (benign):1 | ||||
| chr5:139273953-139274158 | Rare:94 | ||||
| chr5:139293575-139293814 | Rare:77 | ||||
| chr5:139293890-139294012 | Rare:34 | ||||
| chr5:139341679-139341953 | Common:1; Rare:73 | ||||
| chr5:139342194-139342474 | Common:2; Rare:102 | ||||
| chr5:139404050-139404330 | Common:1; Rare:79 | ||||
| chr5:139439446-139439638 | Common:2; Rare:52 | ||||
| chr5:139561088-139561417 | Common:1; Rare:131 | ||||
| chr5:139561728-139561815 | Rare:32 | ||||
| chr5:140043240-140043379 | Rare:35 | ||||
| chr5:140174982-140175284 | Common:2; Rare:80 | ||||
| chr5:140303045-140303173 | Common:1; Rare:44 | ||||
| chr5:140346601-140346896 | Common:1; Rare:76 |