| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:121961875-121962044 | Common:2; Rare:67 | ||||
| chr5:122076896-122077301 | Common:1; Rare:90 | ||||
| chr5:122077353-122077493 | Rare:38; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr5:122077495-122077891 | Common:2; Rare:179; Clinvar:1; Clinvar (benign):6 | ||||
| chr5:122774859-122775115 | Common:1; Rare:96 | ||||
| chr5:122845516-122845621 | Common:3; Rare:40 | ||||
| chr5:123036627-123037032 | Common:2; Rare:108 | ||||
| chr5:123088948-123089249 | Common:11; Rare:131 | ||||
| chr5:123511982-123512280 | Common:1; Rare:81 | ||||
| chr5:124746760-124747002 | Common:5; Rare:44 | ||||
| chr5:124748751-124749046 | Common:3; Rare:65 | ||||
| chr5:126595192-126595322 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):7 | ||||
| chr5:126776917-126777175 | Common:1; Rare:101; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:127030518-127030790 | Common:2; Rare:67 | ||||
| chr5:127290709-127290844 | Rare:29 |