| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10043327-10043647 | Common:4; Rare:132; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:10448391-10448689 | Common:1; Rare:91 | ||||
| chr2:10689901-10690006 | Common:2; Rare:40 | ||||
| chr2:11344958-11345036 | Common:2; Rare:29 | ||||
| chr2:11465821-11466190 | Common:4; Rare:122 | ||||
| chr2:11746369-11746678 | Common:2; Rare:88; Clinvar:5 | ||||
| chr2:12716621-12717062 | Common:3; Rare:135 | ||||
| chr2:17753721-17754168 | Common:4; Rare:142; Clinvar (benign):1 | ||||
| chr2:18560328-18560417 | Rare:26 | ||||
| chr2:18560685-18560801 | Rare:28 | ||||
| chr2:19901634-19901746 | Common:1; Rare:59 | ||||
| chr2:19901944-19902009 | Common:1; Rare:15 | ||||
| chr2:19990043-19990211 | Rare:45 | ||||
| chr2:20051410-20051832 | Common:1; Rare:134 | ||||
| chr2:20446849-20447132 | Common:4; Rare:126 |