| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138575236-138575460 | Common:1; Rare:117 | ||||
| chr5:138575665-138575951 | Rare:81 | ||||
| chr5:138753089-138753134 | Rare:11 | ||||
| chr5:138753220-138753506 | Common:2; Rare:98 | ||||
| chr5:139198274-139198525 | Rare:81; Clinvar (benign):1 | ||||
| chr5:139273971-139274140 | Rare:80 | ||||
| chr5:139293539-139293805 | Rare:88 | ||||
| chr5:139404056-139404230 | Rare:63 | ||||
| chr5:139439446-139439654 | Common:2; Rare:56 | ||||
| chr5:139482651-139482892 | Rare:38 | ||||
| chr5:139561100-139561408 | Common:1; Rare:122 | ||||
| chr5:139561726-139561794 | Rare:32 | ||||
| chr5:139648168-139648368 | Rare:56 | ||||
| chr5:140043121-140043185 | Rare:15 | ||||
| chr5:140107718-140107895 | Rare:57 |