| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132257475-132257755 | Common:8; Rare:74 | ||||
| chr5:132369635-132369740 | Common:2; Rare:29 | ||||
| chr5:132369883-132369964 | Common:2; Rare:31; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:132370147-132370184 | Rare:15; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr5:132410603-132411017 | Common:1; Rare:86 | ||||
| chr5:132490761-132491051 | Rare:75 | ||||
| chr5:132556836-132557053 | Common:1; Rare:77; Clinvar:1 | ||||
| chr5:132777215-132777485 | Rare:69 | ||||
| chr5:132830623-132830740 | Rare:36 | ||||
| chr5:132866435-132866688 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963416-132963746 | Common:2; Rare:92 | ||||
| chr5:133026509-133026759 | Common:4; Rare:65 | ||||
| chr5:133051862-133052216 | Rare:119 | ||||
| chr5:133968571-133968722 | Rare:60 | ||||
| chr5:134004519-134004855 | Common:2; Rare:113 |