| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131796926-131797202 | Rare:83 | ||||
| chr5:132257523-132257703 | Common:6; Rare:38 | ||||
| chr5:132369611-132369740 | Common:2; Rare:35 | ||||
| chr5:132556821-132557020 | Common:1; Rare:70; Clinvar:1 | ||||
| chr5:132866373-132866683 | Common:1; Rare:97; Clinvar (benign):1 | ||||
| chr5:132963275-132963428 | Common:1; Rare:33 | ||||
| chr5:133051851-133052293 | Common:1; Rare:150 | ||||
| chr5:133968573-133968695 | Rare:57 | ||||
| chr5:134004633-134004849 | Common:1; Rare:77 | ||||
| chr5:134225541-134225600 | Common:1; Rare:21 | ||||
| chr5:134226007-134226407 | Common:1; Rare:130 | ||||
| chr5:134371027-134371196 | Common:1; Rare:42 | ||||
| chr5:134371351-134371607 | Common:3; Rare:111 | ||||
| chr5:134411838-134412008 | Rare:62 | ||||
| chr5:134613013-134613266 | Rare:50 |