| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132556800-132557045 | Common:1; Rare:86; Clinvar:1 | ||||
| chr5:132866405-132866686 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963495-132963776 | Rare:74 | ||||
| chr5:133026498-133026728 | Common:3; Rare:68 | ||||
| chr5:133051859-133052107 | Rare:93 | ||||
| chr5:133968525-133968741 | Rare:88 | ||||
| chr5:133980957-133980989 | Rare:5 | ||||
| chr5:134004485-134004893 | Common:3; Rare:136 | ||||
| chr5:134176818-134177248 | Common:4; Rare:136 | ||||
| chr5:134226007-134226412 | Common:1; Rare:130 | ||||
| chr5:134367097-134367226 | Common:1; Rare:40 | ||||
| chr5:134371002-134371190 | Common:1; Rare:50 | ||||
| chr5:134372036-134372236 | Rare:42 | ||||
| chr5:134524013-134524388 | Common:2; Rare:75 | ||||
| chr5:134525490-134525693 | Rare:57 |