| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:159764290-159764573 | Common:2; Rare:82 | ||||
| chr3:160399196-160399309 | Rare:30; Clinvar:1 | ||||
| chr3:160399504-160399687 | Rare:47; Clinvar:1 | ||||
| chr3:160449715-160450027 | Common:2; Rare:105 | ||||
| chr3:160565528-160565842 | Common:2; Rare:115 | ||||
| chr3:160755140-160755175 | Common:1; Rare:13 | ||||
| chr3:160755442-160755629 | Common:1; Rare:66 | ||||
| chr3:161105032-161105354 | Common:3; Rare:96 | ||||
| chr3:167734365-167734683 | Rare:89 | ||||
| chr3:167734810-167735266 | Common:5; Rare:148; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735617-167735778 | Rare:44; Clinvar:1 | ||||
| chr3:168094777-168094970 | Common:1; Rare:37 | ||||
| chr3:169772687-169772817 | Common:1; Rare:34 | ||||
| chr3:169773331-169773459 | Common:1; Rare:41 | ||||
| chr3:169812686-169812996 | Common:1; Rare:51 |