| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:217978722-217978931 | Common:1; Rare:59 | ||||
| chr2:218002839-218003115 | Common:2; Rare:71 | ||||
| chr2:218217057-218217262 | Common:1; Rare:70 | ||||
| chr2:218228574-218228848 | Rare:50 | ||||
| chr2:218270091-218270574 | Common:5; Rare:155; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218279036-218279156 | Rare:46 | ||||
| chr2:218287265-218287411 | Rare:24 | ||||
| chr2:218289992-218290033 | Rare:5 | ||||
| chr2:218399531-218399756 | Common:1; Rare:101 | ||||
| chr2:218568290-218568659 | Common:3; Rare:98 | ||||
| chr2:218659339-218659740 | Common:4; Rare:95 | ||||
| chr2:218671963-218672348 | Common:2; Rare:96 | ||||
| chr2:218782122-218782183 | Rare:17; Clinvar (benign):1 | ||||
| chr2:219176818-219177109 | Common:4; Rare:85 | ||||
| chr2:219177700-219177933 | Common:7; Rare:51 |