| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216081776-216081928 | Common:1; Rare:53 | ||||
| chr2:216371877-216371908 | Rare:8 | ||||
| chr2:216372051-216372223 | Rare:21 | ||||
| chr2:216412247-216412561 | Common:3; Rare:74; Clinvar (benign):2 | ||||
| chr2:216412665-216412786 | Rare:14 | ||||
| chr2:216498686-216499207 | Common:15; Rare:166 | ||||
| chr2:218217058-218217246 | Common:1; Rare:67 | ||||
| chr2:218270086-218270602 | Common:5; Rare:167; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:218287265-218287427 | Common:1; Rare:27 | ||||
| chr2:218568290-218568688 | Common:4; Rare:98 | ||||
| chr2:218659339-218659429 | Common:2; Rare:22 | ||||
| chr2:218659587-218659798 | Rare:58 | ||||
| chr2:218671977-218672334 | Common:2; Rare:89 | ||||
| chr2:219160786-219160875 | Common:1; Rare:32 | ||||
| chr2:219176903-219177109 | Common:4; Rare:63 |