| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52278633-52278811 | Rare:63 | ||||
| chr3:52287755-52287859 | Common:2; Rare:44 | ||||
| chr3:52410410-52410699 | Rare:70 | ||||
| chr3:52455425-52455638 | Common:2; Rare:70 | ||||
| chr3:52533658-52534031 | Common:6; Rare:105 | ||||
| chr3:52536330-52536758 | Common:3; Rare:138 | ||||
| chr3:52685551-52685797 | Common:1; Rare:63 | ||||
| chr3:52685926-52686179 | Common:2; Rare:98 | ||||
| chr3:52705569-52706282 | Common:4; Rare:234 | ||||
| chr3:52770905-52771063 | Common:2; Rare:39 | ||||
| chr3:53130388-53130533 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53229005-53229437 | Common:3; Rare:124 | ||||
| chr3:53235044-53235477 | Common:7; Rare:100 | ||||
| chr3:53255938-53256180 | Common:3; Rare:101 | ||||
| chr3:53347504-53347776 | Common:2; Rare:89 |