| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138575013-138575492 | Common:3; Rare:186 | ||||
| chr5:138575636-138575924 | Rare:80 | ||||
| chr5:138753106-138753498 | Common:2; Rare:128 | ||||
| chr5:139198289-139198519 | Rare:76; Clinvar (benign):1 | ||||
| chr5:139273975-139274150 | Rare:83 | ||||
| chr5:139341803-139342008 | Common:1; Rare:58 | ||||
| chr5:139383268-139383445 | Rare:36 | ||||
| chr5:139561145-139561429 | Common:1; Rare:120 | ||||
| chr5:139561471-139561811 | Rare:126 | ||||
| chr5:139648243-139648422 | Common:1; Rare:61 | ||||
| chr5:140043092-140043405 | Rare:93 | ||||
| chr5:140107988-140108172 | Rare:55 | ||||
| chr5:140303050-140303187 | Common:1; Rare:45 | ||||
| chr5:140401496-140401912 | Common:3; Rare:98 | ||||
| chr5:140402045-140402269 | Common:1; Rare:74 |