| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52239079-52239235 | Common:2; Rare:57 | ||||
| chr3:52278339-52278502 | Rare:65 | ||||
| chr3:52278620-52278777 | Rare:55 | ||||
| chr3:52287737-52287859 | Common:2; Rare:49 | ||||
| chr3:52403247-52403543 | Rare:95; Clinvar:21; Clinvar (benign):15 | ||||
| chr3:52455007-52455150 | Common:4; Rare:14 | ||||
| chr3:52455429-52455734 | Common:2; Rare:100 | ||||
| chr3:52685544-52685804 | Common:2; Rare:67 | ||||
| chr3:52685949-52686072 | Common:2; Rare:52 | ||||
| chr3:52705781-52706192 | Common:2; Rare:144 | ||||
| chr3:52770906-52771007 | Common:2; Rare:28 | ||||
| chr3:53130405-53130533 | Common:1; Rare:40; Clinvar (benign):3 | ||||
| chr3:53347518-53347715 | Common:1; Rare:59 | ||||
| chr3:53846406-53846594 | Rare:64 | ||||
| chr3:53891807-53892040 | Common:2; Rare:72 |