| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160566003-160566016 | Rare:1 | ||||
| chr3:160566079-160566134 | Rare:12 | ||||
| chr3:160755117-160755199 | Common:2; Rare:25 | ||||
| chr3:160755442-160755661 | Common:1; Rare:82 | ||||
| chr3:161221106-161221606 | Common:4; Rare:130 | ||||
| chr3:161221667-161222046 | Common:7; Rare:99 | ||||
| chr3:161371808-161371848 | Rare:4 | ||||
| chr3:161372305-161372529 | Common:2; Rare:34 | ||||
| chr3:167734408-167734720 | Common:1; Rare:89; Clinvar (benign):2 | ||||
| chr3:167734762-167735266 | Common:5; Rare:160; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735512-167735778 | Rare:65; Clinvar:1 | ||||
| chr3:168094844-168095071 | Common:2; Rare:46 | ||||
| chr3:168095838-168096299 | Common:2; Rare:141 | ||||
| chr3:169769277-169769535 | Common:1; Rare:101 | ||||
| chr3:169769543-169769727 | Common:2; Rare:69 |