| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160399174-160399343 | Rare:48; Clinvar:3 | ||||
| chr3:160399474-160399697 | Rare:62; Clinvar:2 | ||||
| chr3:160449516-160449640 | Rare:24 | ||||
| chr3:160565528-160565842 | Common:2; Rare:115 | ||||
| chr3:161105248-161105521 | Common:3; Rare:81 | ||||
| chr3:167734813-167735068 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:168095107-168095223 | Rare:34 | ||||
| chr3:168095842-168096207 | Common:1; Rare:123 | ||||
| chr3:169772731-169772838 | Rare:24 | ||||
| chr3:169773328-169773447 | Rare:41 | ||||
| chr3:169982705-169983254 | Common:2; Rare:117 | ||||
| chr3:170102595-170102903 | Rare:90 | ||||
| chr3:170358200-170358502 | Common:4; Rare:102 | ||||
| chr3:174440818-174441006 | Common:2; Rare:51 | ||||
| chr3:177196448-177196779 | Common:2; Rare:110 |