| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51941931-51942397 | Common:2; Rare:114 | ||||
| chr3:51974895-51975138 | Common:2; Rare:69 | ||||
| chr3:51983287-51983541 | Common:1; Rare:60 | ||||
| chr3:52055843-52056202 | Rare:86 | ||||
| chr3:52197994-52198177 | Common:1; Rare:78 | ||||
| chr3:52239075-52239235 | Common:2; Rare:58 | ||||
| chr3:52246787-52247000 | Common:1; Rare:58 | ||||
| chr3:52278620-52278777 | Rare:55 | ||||
| chr3:52287749-52287871 | Common:2; Rare:51 | ||||
| chr3:52410015-52410216 | Rare:50 | ||||
| chr3:52455414-52455734 | Common:2; Rare:102 | ||||
| chr3:52685544-52685647 | Rare:32 | ||||
| chr3:52685772-52686118 | Common:3; Rare:130 | ||||
| chr3:52705576-52706276 | Common:4; Rare:230 | ||||
| chr3:53130396-53130533 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):3 |