| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792676-9793124 | Common:3; Rare:157 | ||||
| chr3:9890508-9890685 | Common:2; Rare:66 | ||||
| chr3:9916960-9917186 | Common:2; Rare:47 | ||||
| chr3:9933673-9933868 | Common:1; Rare:76 | ||||
| chr3:9933967-9934065 | Rare:23 | ||||
| chr3:9986777-9987167 | Common:3; Rare:109 | ||||
| chr3:10026268-10026480 | Common:1; Rare:68 | ||||
| chr3:10115518-10115748 | Common:4; Rare:83 | ||||
| chr3:10141655-10141955 | Common:2; Rare:135; Clinvar:33; Clinvar (benign):26 | ||||
| chr3:10321030-10321124 | Rare:52 | ||||
| chr3:11846843-11847027 | Common:1; Rare:52 | ||||
| chr3:12287739-12288000 | Common:7; Rare:52 | ||||
| chr3:12484333-12484529 | Common:5; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:12556904-12557173 | Common:5; Rare:93 | ||||
| chr3:12664075-12664352 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):3 |