| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132257477-132257823 | Common:8; Rare:88 | ||||
| chr5:132294107-132294441 | Common:1; Rare:78 | ||||
| chr5:132410603-132410987 | Common:1; Rare:78 | ||||
| chr5:132557352-132557444 | Rare:23; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr5:132866435-132866711 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963262-132963468 | Common:3; Rare:50 | ||||
| chr5:132963482-132963803 | Common:1; Rare:81 | ||||
| chr5:133051861-133052107 | Rare:92 | ||||
| chr5:133968525-133968741 | Rare:88 | ||||
| chr5:134004482-134004827 | Common:3; Rare:113 | ||||
| chr5:134004895-134005074 | Rare:38 | ||||
| chr5:134176690-134177051 | Common:9; Rare:130 | ||||
| chr5:134225522-134225790 | Common:2; Rare:96 | ||||
| chr5:134225847-134226410 | Common:3; Rare:177 | ||||
| chr5:134367141-134367231 | Common:1; Rare:27 |