| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132490764-132491020 | Rare:67 | ||||
| chr5:132556784-132557012 | Common:1; Rare:75; Clinvar:1 | ||||
| chr5:132866471-132866698 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133051862-133052306 | Common:1; Rare:144 | ||||
| chr5:133968551-133968815 | Common:1; Rare:102 | ||||
| chr5:134004654-134004893 | Common:1; Rare:90 | ||||
| chr5:134004923-134005104 | Rare:37 | ||||
| chr5:134226039-134226142 | Common:1; Rare:36 | ||||
| chr5:134371027-134371184 | Common:1; Rare:40 | ||||
| chr5:134411846-134412008 | Rare:56 | ||||
| chr5:134648726-134648816 | Rare:20 | ||||
| chr5:134738412-134738609 | Rare:76 | ||||
| chr5:134758579-134758819 | Common:1; Rare:82 | ||||
| chr5:134845824-134846089 | Rare:119 | ||||
| chr5:134874261-134874418 | Common:1; Rare:81 |