| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:136992895-136993103 | Rare:34 | ||||
| chr5:137735851-137735916 | Common:1; Rare:11; Clinvar (benign):1 | ||||
| chr5:137867780-137867901 | Rare:21 | ||||
| chr5:137880330-137880725 | Common:1; Rare:64 | ||||
| chr5:137888892-137888994 | Common:1; Rare:26 | ||||
| chr5:137889288-137889458 | Common:1; Rare:61 | ||||
| chr5:138033012-138033193 | Common:1; Rare:67 | ||||
| chr5:138178604-138178739 | Rare:32 | ||||
| chr5:138178923-138179178 | Common:3; Rare:54 | ||||
| chr5:138338002-138338296 | Common:2; Rare:122 | ||||
| chr5:138465796-138465856 | Rare:21 | ||||
| chr5:138543085-138543570 | Common:2; Rare:159 | ||||
| chr5:138575243-138575480 | Common:1; Rare:121 | ||||
| chr5:138575667-138575749 | Rare:21 | ||||
| chr5:138753268-138753507 | Common:2; Rare:81 |