| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:127517507-127517651 | Common:5; Rare:66 | ||||
| chr5:132227805-132227889 | Common:2; Rare:20 | ||||
| chr5:133051640-133052113 | Common:2; Rare:169 | ||||
| chr5:133968591-133968737 | Rare:51 | ||||
| chr5:134004535-134004827 | Common:1; Rare:95 | ||||
| chr5:134411846-134412002 | Rare:51 | ||||
| chr5:134738418-134738573 | Rare:55 | ||||
| chr5:138178946-138179177 | Common:3; Rare:48 | ||||
| chr5:139439453-139439637 | Common:2; Rare:50 | ||||
| chr5:140557437-140557548 | Common:2; Rare:67 | ||||
| chr5:140647631-140647876 | Common:4; Rare:97; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:140691309-140691614 | Common:1; Rare:106; Clinvar:8 | ||||
| chr5:151080985-151081190 | Common:1; Rare:66 | ||||
| chr5:154038873-154038989 | Common:1; Rare:38 | ||||
| chr5:154941031-154941107 | Common:1; Rare:32 |