| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134226002-134226407 | Common:1; Rare:133 | ||||
| chr5:134371031-134371182 | Common:1; Rare:39 | ||||
| chr5:134411846-134412002 | Rare:51 | ||||
| chr5:134632745-134632937 | Rare:38 | ||||
| chr5:134648689-134648816 | Rare:37 | ||||
| chr5:134738436-134738577 | Rare:54 | ||||
| chr5:135399133-135399482 | Common:1; Rare:83 | ||||
| chr5:137867564-137867890 | Rare:65 | ||||
| chr5:137880333-137880724 | Common:1; Rare:63 | ||||
| chr5:137888892-137888994 | Common:1; Rare:26 | ||||
| chr5:137889298-137889457 | Common:1; Rare:56 | ||||
| chr5:138178604-138178767 | Rare:37 | ||||
| chr5:138543095-138543496 | Common:2; Rare:118 | ||||
| chr5:138753255-138753503 | Common:2; Rare:87 | ||||
| chr5:139198277-139198528 | Rare:82; Clinvar (benign):1 |