| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138338203-138338277 | Common:1; Rare:33 | ||||
| chr5:138543110-138543512 | Common:2; Rare:124 | ||||
| chr5:138575319-138575480 | Common:1; Rare:83 | ||||
| chr5:138753280-138753505 | Common:2; Rare:75 | ||||
| chr5:139273978-139274133 | Rare:72 | ||||
| chr5:139404056-139404218 | Rare:59 | ||||
| chr5:139561732-139561794 | Rare:28 | ||||
| chr5:140303057-140303145 | Common:1; Rare:30 | ||||
| chr5:140557437-140557548 | Common:2; Rare:67 | ||||
| chr5:140564573-140564837 | Rare:73 | ||||
| chr5:140639302-140639489 | Common:3; Rare:50 | ||||
| chr5:140647579-140647883 | Common:5; Rare:124; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664775-140664874 | Rare:20 | ||||
| chr5:140691313-140691515 | Common:1; Rare:77; Clinvar:7 | ||||
| chr5:141320732-141320928 | Common:3; Rare:67 |