| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52239079-52239235 | Common:2; Rare:57 | ||||
| chr3:52278628-52278777 | Rare:52 | ||||
| chr3:52287749-52288085 | Common:3; Rare:116 | ||||
| chr3:52455425-52455642 | Common:2; Rare:72 | ||||
| chr3:52536330-52536752 | Common:3; Rare:135 | ||||
| chr3:52685789-52686187 | Common:3; Rare:150 | ||||
| chr3:52705768-52706217 | Common:2; Rare:157 | ||||
| chr3:53130396-53130523 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53347517-53347763 | Common:2; Rare:80 | ||||
| chr3:53891794-53892075 | Common:4; Rare:94 | ||||
| chr3:54123421-54123470 | Rare:10 | ||||
| chr3:55481198-55481492 | Common:1; Rare:80 | ||||
| chr3:56557076-56557238 | Common:2; Rare:63 | ||||
| chr3:56683257-56683358 | Common:2; Rare:31 | ||||
| chr3:56801902-56802030 | Rare:48 |