| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157436789-157437049 | Common:2; Rare:65; Clinvar:1 | ||||
| chr3:158105728-158105920 | Common:5; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:160399175-160399307 | Rare:35; Clinvar:2 | ||||
| chr3:160399509-160399669 | Rare:36 | ||||
| chr3:160565417-160565845 | Common:2; Rare:155 | ||||
| chr3:167734832-167735084 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735626-167735744 | Rare:31 | ||||
| chr3:169769549-169769615 | Rare:29 | ||||
| chr3:169769633-169769731 | Common:2; Rare:33 | ||||
| chr3:169773328-169773438 | Rare:36 | ||||
| chr3:170870183-170870320 | Rare:62 | ||||
| chr3:179347573-179347753 | Common:1; Rare:38 | ||||
| chr3:179604626-179604841 | Common:1; Rare:74 | ||||
| chr3:183884807-183884972 | Rare:70 | ||||
| chr3:184135270-184135385 | Common:2; Rare:30; Clinvar:1 |