| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138338230-138338267 | Common:1; Rare:22 | ||||
| chr5:138465772-138466078 | Rare:132 | ||||
| chr5:138543070-138543549 | Common:3; Rare:148 | ||||
| chr5:138558572-138558741 | Common:1; Rare:46; Clinvar:1 | ||||
| chr5:138753268-138753507 | Common:2; Rare:81 | ||||
| chr5:139198284-139198527 | Rare:82; Clinvar (benign):1 | ||||
| chr5:139273975-139274135 | Rare:75 | ||||
| chr5:139293528-139293805 | Rare:92 | ||||
| chr5:139384493-139384685 | Common:1; Rare:45 | ||||
| chr5:139404050-139404232 | Rare:64 | ||||
| chr5:139439453-139439646 | Common:2; Rare:52 | ||||
| chr5:139561244-139561559 | Rare:125 | ||||
| chr5:139561732-139561802 | Rare:29 | ||||
| chr5:140107679-140107846 | Rare:57 | ||||
| chr5:140175017-140175275 | Common:1; Rare:63 |