| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134371435-134371586 | Common:3; Rare:68 | ||||
| chr5:134411850-134412008 | Rare:53 | ||||
| chr5:134524307-134524407 | Rare:19 | ||||
| chr5:134648668-134648817 | Rare:43 | ||||
| chr5:134738423-134738713 | Common:1; Rare:121 | ||||
| chr5:134905018-134905197 | Common:1; Rare:48 | ||||
| chr5:135033405-135033503 | Rare:21 | ||||
| chr5:136132741-136132950 | Common:1; Rare:66 | ||||
| chr5:137880335-137880731 | Common:2; Rare:67 | ||||
| chr5:137889320-137889457 | Common:1; Rare:45 | ||||
| chr5:138032971-138033193 | Common:1; Rare:78 | ||||
| chr5:138542888-138543513 | Common:3; Rare:190 | ||||
| chr5:138575300-138575443 | Common:1; Rare:81 | ||||
| chr5:138753277-138753507 | Common:2; Rare:77 | ||||
| chr5:139198258-139198531 | Rare:84; Clinvar (benign):1 |