| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:161371925-161372076 | Rare:37 | ||||
| chr3:165195727-165195811 | Rare:20 | ||||
| chr3:167734804-167735280 | Common:5; Rare:155; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735608-167735784 | Rare:47; Clinvar:1 | ||||
| chr3:169772762-169772808 | Rare:9 | ||||
| chr3:169773369-169773418 | Rare:13 | ||||
| chr3:169812498-169812745 | Common:2; Rare:60 | ||||
| chr3:169966647-169966858 | Common:1; Rare:84 | ||||
| chr3:170418690-170419021 | Common:1; Rare:72 | ||||
| chr3:170870166-170870282 | Rare:64 | ||||
| chr3:171460101-171460209 | Rare:26 | ||||
| chr3:171460221-171460532 | Common:2; Rare:69 | ||||
| chr3:171460771-171460904 | Rare:30 | ||||
| chr3:172039435-172039656 | Common:1; Rare:68 | ||||
| chr3:172711063-172711143 | Rare:36 |