| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:126423316-126423571 | Rare:106 | ||||
| chr5:126595132-126595372 | Common:10; Rare:208; Clinvar:11; Clinvar (benign):21; Clinvar (pathogenic):6 | ||||
| chr5:126600819-126600988 | Common:1; Rare:134 | ||||
| chr5:126776867-126777421 | Common:7; Rare:308; Clinvar:8; Clinvar (benign):13 | ||||
| chr5:127030420-127030800 | Common:6; Rare:150 | ||||
| chr5:127517472-127517768 | Common:14; Rare:239 | ||||
| chr5:128083569-128083772 | Common:4; Rare:137 | ||||
| chr5:128538196-128538427 | Common:5; Rare:74 | ||||
| chr5:129094469-129094761 | Common:6; Rare:234 | ||||
| chr5:131165097-131165409 | Common:5; Rare:211; Clinvar (benign):3 | ||||
| chr5:131170660-131171021 | Common:2; Rare:160; Clinvar (benign):4 | ||||
| chr5:131263805-131264155 | Common:3; Rare:225 | ||||
| chr5:131635072-131635635 | Common:2; Rare:283 | ||||
| chr5:131796928-131797266 | Rare:181 | ||||
| chr5:132227744-132227955 | Common:4; Rare:91 |