| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138178941-138179188 | Common:3; Rare:50 | ||||
| chr5:138331783-138332142 | Common:2; Rare:87 | ||||
| chr5:138543095-138543518 | Common:2; Rare:129 | ||||
| chr5:138575304-138575463 | Common:1; Rare:87 | ||||
| chr5:138753255-138753488 | Common:2; Rare:81 | ||||
| chr5:139198277-139198526 | Rare:82; Clinvar (benign):1 | ||||
| chr5:139273975-139274140 | Rare:77 | ||||
| chr5:139293528-139293803 | Rare:92 | ||||
| chr5:139341675-139341943 | Common:1; Rare:73 | ||||
| chr5:139404007-139404198 | Rare:67 | ||||
| chr5:139439453-139439656 | Common:2; Rare:54 | ||||
| chr5:139561100-139561358 | Common:1; Rare:101 | ||||
| chr5:139561733-139561800 | Rare:28 | ||||
| chr5:139659207-139659360 | Rare:39 | ||||
| chr5:140174867-140175208 | Rare:105 |