| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:151020428-151020738 | Common:2; Rare:79 | ||||
| chr5:151025105-151025492 | Common:1; Rare:81 | ||||
| chr5:151080935-151081183 | Common:1; Rare:80 | ||||
| chr5:151771412-151771580 | Rare:52 | ||||
| chr5:154038873-154039015 | Common:1; Rare:51 | ||||
| chr5:154445782-154445966 | Common:1; Rare:45 | ||||
| chr5:154755728-154756076 | Common:3; Rare:78 | ||||
| chr5:154834985-154835239 | Rare:42 | ||||
| chr5:154857777-154857891 | Rare:32 | ||||
| chr5:154858058-154858290 | Common:6; Rare:73 | ||||
| chr5:154858471-154858729 | Common:1; Rare:85 | ||||
| chr5:156326990-156327215 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:157382921-157383241 | Common:1; Rare:54 | ||||
| chr5:157575748-157575926 | Common:3; Rare:46 | ||||
| chr5:157731373-157731462 | Common:3; Rare:37 |