| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140557364-140557519 | Common:2; Rare:189 | ||||
| chr5:140564309-140564478 | Common:2; Rare:90 | ||||
| chr5:140564543-140564853 | Rare:157 | ||||
| chr5:140639154-140639638 | Common:6; Rare:180 | ||||
| chr5:140639655-140640055 | Rare:170 | ||||
| chr5:140647547-140647886 | Common:10; Rare:263; Clinvar:8; Clinvar (benign):7 | ||||
| chr5:140664719-140664932 | Common:5; Rare:114 | ||||
| chr5:140691290-140691664 | Common:2; Rare:267; Clinvar:24; Clinvar (benign):3 | ||||
| chr5:140700214-140700470 | Rare:145 | ||||
| chr5:141320730-141320922 | Common:4; Rare:131 | ||||
| chr5:141618891-141619275 | Common:1; Rare:191; Clinvar:10; Clinvar (benign):2 | ||||
| chr5:141636778-141637012 | Common:4; Rare:189 | ||||
| chr5:141651367-141651478 | Rare:39 | ||||
| chr5:141651383-141651490 | Rare:33 | ||||
| chr5:141682191-141682355 | Common:2; Rare:98 |