| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131796936-131797221 | Rare:81 | ||||
| chr5:132866318-132866678 | Common:1; Rare:107 | ||||
| chr5:133051862-133052125 | Rare:96 | ||||
| chr5:133968560-133968722 | Rare:67 | ||||
| chr5:134004521-134004851 | Common:1; Rare:112 | ||||
| chr5:134004913-134005005 | Rare:21 | ||||
| chr5:134371027-134371231 | Common:1; Rare:49 | ||||
| chr5:134371430-134371601 | Common:3; Rare:76 | ||||
| chr5:134648688-134648816 | Rare:37 | ||||
| chr5:134738291-134738577 | Rare:97 | ||||
| chr5:134874217-134874423 | Common:1; Rare:98 | ||||
| chr5:135399105-135399346 | Rare:63 | ||||
| chr5:135578987-135579186 | Common:2; Rare:54 | ||||
| chr5:137867688-137867952 | Common:1; Rare:44; Clinvar (benign):2 | ||||
| chr5:138178941-138179154 | Common:2; Rare:46 |