| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34929538-34929915 | Rare:137 | ||||
| chr5:36151881-36152187 | Rare:98 | ||||
| chr5:36242126-36242435 | Common:2; Rare:85 | ||||
| chr5:36876650-36876907 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37249317-37249562 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371040-37371207 | Rare:59 | ||||
| chr5:38845746-38846067 | Common:2; Rare:85 | ||||
| chr5:39074350-39074505 | Common:1; Rare:68 | ||||
| chr5:40679298-40679419 | Common:1; Rare:25 | ||||
| chr5:40679698-40679929 | Common:1; Rare:48 | ||||
| chr5:40755866-40756018 | Rare:41 | ||||
| chr5:40798158-40798401 | Common:1; Rare:89 | ||||
| chr5:40835173-40835389 | Common:2; Rare:85 | ||||
| chr5:43120828-43120950 | Common:2; Rare:58 | ||||
| chr5:43121416-43121648 | Common:1; Rare:87 |