| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179322783-179323115 | Common:10; Rare:193 | ||||
| chr3:179347569-179347792 | Common:2; Rare:86 | ||||
| chr3:179451391-179451567 | Common:2; Rare:105 | ||||
| chr3:179562658-179563083 | Rare:246 | ||||
| chr3:179604575-179604916 | Common:6; Rare:234 | ||||
| chr3:179652953-179653293 | Common:2; Rare:108 | ||||
| chr3:180602052-180602370 | Common:2; Rare:173 | ||||
| chr3:180912350-180912736 | Common:7; Rare:242 | ||||
| chr3:180989416-180989900 | Rare:260; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:182793324-182793692 | Common:6; Rare:171 | ||||
| chr3:182980468-182980630 | Rare:92 | ||||
| chr3:183099438-183099720 | Common:2; Rare:94; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183428530-183428840 | Common:3; Rare:93 | ||||
| chr3:183635497-183635709 | Common:4; Rare:116 | ||||
| chr3:183636370-183636890 | Common:5; Rare:210 |