| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167734837-167735222 | Common:3; Rare:122; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:169773128-169773427 | Common:1; Rare:93 | ||||
| chr3:169966706-169966858 | Rare:65 | ||||
| chr3:170870175-170870312 | Rare:65 | ||||
| chr3:172711051-172711214 | Rare:60 | ||||
| chr3:172750578-172750787 | Common:3; Rare:61 | ||||
| chr3:179347546-179347785 | Common:2; Rare:57 | ||||
| chr3:179604614-179604846 | Common:2; Rare:84 | ||||
| chr3:180602054-180602258 | Common:1; Rare:72 | ||||
| chr3:180912372-180912688 | Common:3; Rare:110 | ||||
| chr3:180989647-180989779 | Rare:58; Clinvar:1 | ||||
| chr3:182793376-182793673 | Common:3; Rare:70 | ||||
| chr3:182980491-182980750 | Rare:90 | ||||
| chr3:183099460-183099742 | Common:2; Rare:87; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183555688-183555770 | Rare:16 |