| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167735586-167735740 | Rare:37 | ||||
| chr3:169773341-169773424 | Rare:25 | ||||
| chr3:170908590-170908837 | Common:1; Rare:68 | ||||
| chr3:171460320-171460571 | Rare:57 | ||||
| chr3:179148028-179148202 | Common:3; Rare:61 | ||||
| chr3:179604605-179604936 | Common:3; Rare:131 | ||||
| chr3:180967897-180968269 | Rare:97 | ||||
| chr3:180989606-180989847 | Rare:101; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183099436-183099692 | Common:2; Rare:88; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183253852-183254165 | Common:2; Rare:94 | ||||
| chr3:183635473-183635763 | Common:5; Rare:83 | ||||
| chr3:184017870-184018103 | Common:1; Rare:72 | ||||
| chr3:184135248-184135394 | Common:2; Rare:40; Clinvar:2 | ||||
| chr3:184185856-184186226 | Common:5; Rare:142 | ||||
| chr3:184248910-184249029 | Rare:57; Clinvar:4; Clinvar (benign):1 |