| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218270054-218270565 | Common:5; Rare:160; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:218323118-218323374 | Common:2; Rare:99 | ||||
| chr2:218398573-218398745 | Common:2; Rare:61 | ||||
| chr2:218400263-218400300 | Rare:18 | ||||
| chr2:218424123-218424348 | Common:1; Rare:48 | ||||
| chr2:218568252-218568622 | Common:3; Rare:100 | ||||
| chr2:218568767-218568961 | Common:1; Rare:61 | ||||
| chr2:218659339-218659363 | Rare:8 | ||||
| chr2:218659600-218659743 | Rare:34 | ||||
| chr2:218671977-218672339 | Common:2; Rare:89 | ||||
| chr2:218782087-218782199 | Rare:27; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218984459-218984588 | Rare:24 | ||||
| chr2:219160778-219160966 | Common:1; Rare:51 | ||||
| chr2:219169993-219170260 | Rare:59 | ||||
| chr2:219176897-219177109 | Common:4; Rare:64 |