| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:139389568-139389876 | Common:2; Rare:98 | ||||
| chr3:139539477-139539552 | Rare:24 | ||||
| chr3:139539554-139539788 | Common:3; Rare:75 | ||||
| chr3:140941655-140941882 | Common:2; Rare:84 | ||||
| chr3:141231644-141231863 | Common:2; Rare:72 | ||||
| chr3:141368218-141368540 | Rare:65 | ||||
| chr3:141486879-141487085 | Common:1; Rare:68 | ||||
| chr3:142447974-142448163 | Common:1; Rare:73 | ||||
| chr3:142578711-142578959 | Rare:89; Clinvar:1 | ||||
| chr3:143001436-143001638 | Common:3; Rare:74 | ||||
| chr3:146160975-146161386 | Common:2; Rare:125; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:149129545-149129676 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:149377536-149377857 | Common:1; Rare:81 | ||||
| chr3:149576207-149576358 | Rare:24 | ||||
| chr3:149657964-149658183 | Rare:46 |