| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216695523-216695681 | Rare:29 | ||||
| chr2:217978616-217978755 | Rare:39 | ||||
| chr2:217978813-217978941 | Common:1; Rare:36 | ||||
| chr2:218217064-218217246 | Common:1; Rare:66 | ||||
| chr2:218270082-218270565 | Common:5; Rare:153; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:218292490-218292604 | Rare:28 | ||||
| chr2:218322988-218323374 | Common:6; Rare:133 | ||||
| chr2:218568269-218568708 | Common:5; Rare:115 | ||||
| chr2:218568733-218568956 | Common:1; Rare:63 | ||||
| chr2:218659339-218659748 | Common:4; Rare:96 | ||||
| chr2:218671977-218672374 | Common:2; Rare:100 | ||||
| chr2:218710701-218711005 | Common:3; Rare:72 | ||||
| chr2:219176856-219177109 | Common:4; Rare:78 | ||||
| chr2:219206683-219206916 | Rare:86 | ||||
| chr2:219229330-219229416 | Rare:28 |