| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160565569-160565784 | Common:1; Rare:74 | ||||
| chr3:161221172-161221330 | Rare:50 | ||||
| chr3:167734820-167735254 | Common:5; Rare:139; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:169773305-169773418 | Rare:39 | ||||
| chr3:169966706-169966842 | Rare:58 | ||||
| chr3:172711011-172711374 | Common:1; Rare:105 | ||||
| chr3:172750883-172751026 | Rare:43 | ||||
| chr3:177196411-177196586 | Rare:56 | ||||
| chr3:179604620-179604816 | Common:1; Rare:64 | ||||
| chr3:180912343-180912713 | Common:4; Rare:122 | ||||
| chr3:180989628-180989782 | Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183635514-183635661 | Common:1; Rare:44 | ||||
| chr3:184135221-184135385 | Common:2; Rare:48; Clinvar:5 | ||||
| chr3:184185857-184186218 | Common:5; Rare:138 | ||||
| chr3:184249518-184249682 | Rare:42 |