| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:128082982-128083179 | Common:8; Rare:62 | ||||
| chr5:128084548-128084678 | Rare:39 | ||||
| chr5:131548297-131548454 | Common:1; Rare:40 | ||||
| chr5:132426644-132426712 | Rare:12 | ||||
| chr5:132471688-132471942 | Common:1; Rare:45 | ||||
| chr5:134927162-134927176 | Rare:3 | ||||
| chr5:135350047-135350171 | Rare:20 | ||||
| chr5:135354097-135354357 | Common:2; Rare:39 | ||||
| chr5:135354708-135354743 | Rare:8 | ||||
| chr5:138933670-138933971 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:138962001-138962126 | Common:1; Rare:15 | ||||
| chr5:140109267-140109520 | Rare:34 | ||||
| chr5:140257579-140257845 | Rare:38 | ||||
| chr5:140261607-140261829 | Rare:38 | ||||
| chr5:140553435-140553703 | Rare:46 |