| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179147996-179148182 | Common:2; Rare:63 | ||||
| chr3:179322736-179322927 | Common:5; Rare:45 | ||||
| chr3:179347588-179347799 | Common:1; Rare:51 | ||||
| chr3:179451381-179451582 | Common:1; Rare:70 | ||||
| chr3:179562614-179563052 | Rare:144 | ||||
| chr3:179563140-179563305 | Rare:51 | ||||
| chr3:179604610-179604877 | Common:2; Rare:104 | ||||
| chr3:179974258-179974328 | Common:1; Rare:9 | ||||
| chr3:180036739-180036833 | Rare:28 | ||||
| chr3:180036849-180037222 | Common:1; Rare:102 | ||||
| chr3:180602014-180602326 | Common:1; Rare:104 | ||||
| chr3:180602469-180602589 | Rare:28 | ||||
| chr3:180912331-180912722 | Common:4; Rare:129 | ||||
| chr3:180989528-180989863 | Rare:132; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:182980493-182980790 | Common:1; Rare:104 |