| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52154379-52154473 | Common:1; Rare:31 | ||||
| chr3:52239000-52239268 | Common:2; Rare:89 | ||||
| chr3:52287759-52287873 | Common:2; Rare:46 | ||||
| chr3:52288015-52288063 | Rare:17 | ||||
| chr3:52403279-52403589 | Rare:94; Clinvar:17; Clinvar (benign):14 | ||||
| chr3:52455328-52455686 | Common:2; Rare:107 | ||||
| chr3:52525015-52525316 | Common:9; Rare:132 | ||||
| chr3:52527295-52527725 | Common:3; Rare:127 | ||||
| chr3:52528012-52528202 | Rare:67 | ||||
| chr3:52533507-52534039 | Common:7; Rare:141 | ||||
| chr3:52534227-52534252 | Rare:3 | ||||
| chr3:52534518-52534872 | Common:3; Rare:82 | ||||
| chr3:52536840-52536899 | Rare:13 | ||||
| chr3:52685539-52685726 | Rare:56 | ||||
| chr3:52685752-52686121 | Common:3; Rare:133 |