| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51975048-51975136 | Common:1; Rare:32 | ||||
| chr3:51983145-51983541 | Common:1; Rare:88 | ||||
| chr3:51995740-51996042 | Common:3; Rare:96 | ||||
| chr3:52239079-52239255 | Common:2; Rare:64 | ||||
| chr3:52278625-52278759 | Rare:48 | ||||
| chr3:52287755-52287859 | Common:2; Rare:44 | ||||
| chr3:52455400-52455734 | Common:2; Rare:105 | ||||
| chr3:52495282-52495416 | Common:1; Rare:40 | ||||
| chr3:52535011-52535129 | Common:1; Rare:25 | ||||
| chr3:52685752-52686143 | Common:3; Rare:141 | ||||
| chr3:52705569-52706270 | Common:4; Rare:229 | ||||
| chr3:53130410-53130523 | Common:1; Rare:35; Clinvar (benign):2 | ||||
| chr3:53347516-53347734 | Common:2; Rare:69 | ||||
| chr3:53891807-53892014 | Common:2; Rare:65 | ||||
| chr3:56557086-56557238 | Common:2; Rare:60 |