| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216081788-216081871 | Rare:22 | ||||
| chr2:216498754-216498898 | Common:4; Rare:65 | ||||
| chr2:218216859-218217226 | Common:2; Rare:107 | ||||
| chr2:218270106-218270541 | Common:5; Rare:133; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218568301-218568615 | Common:2; Rare:86 | ||||
| chr2:218568726-218568957 | Common:1; Rare:64 | ||||
| chr2:218659606-218659733 | Rare:30 | ||||
| chr2:218671974-218672334 | Common:2; Rare:90 | ||||
| chr2:219176926-219177114 | Common:4; Rare:58 | ||||
| chr2:219206687-219206923 | Rare:85 | ||||
| chr2:219229581-219229875 | Common:2; Rare:79 | ||||
| chr2:219245407-219245511 | Rare:26 | ||||
| chr2:219498670-219498938 | Common:2; Rare:60 | ||||
| chr2:227325191-227325385 | Common:5; Rare:67 | ||||
| chr2:227813666-227813877 | Rare:36 |