| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140700272-140700473 | Rare:66 | ||||
| chr5:140827819-140827985 | Rare:31 | ||||
| chr5:140926090-140926430 | Common:1; Rare:107 | ||||
| chr5:140966270-140966640 | Common:1; Rare:94 | ||||
| chr5:141051584-141051726 | Rare:49 | ||||
| chr5:141094429-141094655 | Rare:51 | ||||
| chr5:141172517-141172644 | Common:1; Rare:24 | ||||
| chr5:141245394-141245906 | Common:4; Rare:187 | ||||
| chr5:141320752-141320967 | Common:2; Rare:72 | ||||
| chr5:141407651-141408100 | Rare:126 | ||||
| chr5:141475835-141475969 | Rare:28 | ||||
| chr5:141560783-141560936 | Common:2; Rare:37 | ||||
| chr5:141618921-141619299 | Common:1; Rare:119; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:141636838-141637047 | Common:1; Rare:73 | ||||
| chr5:141637196-141638055 | Common:4; Rare:250 |