| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52454100-52454177 | Common:1; Rare:12 | ||||
| chr3:52455427-52455638 | Common:2; Rare:70 | ||||
| chr3:52524847-52525081 | Common:2; Rare:111 | ||||
| chr3:52536304-52536752 | Common:4; Rare:137 | ||||
| chr3:52685544-52685648 | Rare:32 | ||||
| chr3:52685825-52686213 | Common:2; Rare:146 | ||||
| chr3:52705702-52706223 | Common:3; Rare:176 | ||||
| chr3:52706384-52706459 | Rare:21 | ||||
| chr3:52770913-52771077 | Common:2; Rare:45 | ||||
| chr3:53130396-53130568 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53347477-53347734 | Common:2; Rare:94 | ||||
| chr3:53495248-53495393 | Rare:45 | ||||
| chr3:53846417-53846585 | Rare:55 | ||||
| chr3:53881782-53881817 | Rare:6 | ||||
| chr3:53882051-53882354 | Common:5; Rare:105 |