| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:124748777-124748997 | Common:2; Rare:52 | ||||
| chr5:126595160-126595304 | Common:1; Rare:74; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr5:127290706-127290839 | Rare:29 | ||||
| chr5:127517527-127517716 | Common:4; Rare:83 | ||||
| chr5:131170670-131170993 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr5:131635196-131635374 | Common:1; Rare:65 | ||||
| chr5:132737516-132737608 | Rare:28 | ||||
| chr5:133051862-133052114 | Rare:94 | ||||
| chr5:134004648-134004890 | Common:1; Rare:90 | ||||
| chr5:134411858-134412008 | Rare:48 | ||||
| chr5:134648726-134648816 | Rare:20 | ||||
| chr5:134874268-134874418 | Common:1; Rare:77 | ||||
| chr5:138178615-138178724 | Rare:28 | ||||
| chr5:138178953-138179178 | Common:2; Rare:47 | ||||
| chr5:138331759-138332127 | Common:2; Rare:91 |