| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218270091-218270565 | Common:5; Rare:149; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:218287265-218287427 | Common:1; Rare:27 | ||||
| chr2:218568293-218568688 | Common:4; Rare:98 | ||||
| chr2:218568767-218568929 | Common:1; Rare:48 | ||||
| chr2:218659518-218659738 | Common:1; Rare:54 | ||||
| chr2:218671977-218672061 | Rare:29 | ||||
| chr2:218710709-218710888 | Common:2; Rare:50 | ||||
| chr2:219176926-219177073 | Common:4; Rare:45 | ||||
| chr2:219206608-219206923 | Rare:117 | ||||
| chr2:219229577-219229891 | Common:2; Rare:95 | ||||
| chr2:219245416-219245511 | Rare:24 | ||||
| chr2:219279225-219279541 | Common:3; Rare:100; Clinvar (benign):1 | ||||
| chr2:219418614-219419040 | Common:2; Rare:143; Clinvar:32; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr2:219419811-219420189 | Common:2; Rare:80; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr2:219420491-219420953 | Common:2; Rare:126; Clinvar:16; Clinvar (benign):16; Clinvar (pathogenic):4 |