| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:122077355-122077491 | Rare:37; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr5:122129451-122129581 | Common:1; Rare:36 | ||||
| chr5:122311625-122311757 | Common:3; Rare:27 | ||||
| chr5:122774856-122775117 | Common:1; Rare:100 | ||||
| chr5:122845315-122845639 | Common:3; Rare:112 | ||||
| chr5:123511981-123512192 | Common:1; Rare:54 | ||||
| chr5:124745995-124746156 | Common:1; Rare:37 | ||||
| chr5:124746262-124746705 | Common:2; Rare:81 | ||||
| chr5:124748740-124749019 | Common:3; Rare:63 | ||||
| chr5:126423324-126423584 | Rare:69 | ||||
| chr5:126595183-126595327 | Common:2; Rare:69; Clinvar:4; Clinvar (benign):7 | ||||
| chr5:127030511-127030755 | Common:2; Rare:58 | ||||
| chr5:127290677-127290873 | Rare:39 | ||||
| chr5:131170698-131171006 | Common:1; Rare:64; Clinvar (benign):2 | ||||
| chr5:131263908-131264125 | Rare:79 |