| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3575107-3575448 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:3594681-3595165 | Common:3; Rare:135 | ||||
| chr2:6917331-6917527 | Rare:72 | ||||
| chr2:8679074-8679261 | Rare:68 | ||||
| chr2:8837555-8837734 | Common:1; Rare:70 | ||||
| chr2:9423129-9423709 | Common:1; Rare:158 | ||||
| chr2:9474491-9474630 | Common:6; Rare:63 | ||||
| chr2:9555719-9555926 | Common:2; Rare:68 | ||||
| chr2:9630944-9631344 | Common:3; Rare:127 | ||||
| chr2:9843160-9843539 | Common:7; Rare:117 | ||||
| chr2:9843666-9843743 | Common:3; Rare:31 | ||||
| chr2:10043318-10043752 | Common:4; Rare:186; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:10448391-10448689 | Common:1; Rare:91 | ||||
| chr2:10689910-10690018 | Common:2; Rare:37 | ||||
| chr2:10812685-10813034 | Common:5; Rare:130 |