| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218323004-218323361 | Common:6; Rare:123 | ||||
| chr2:218398094-218398239 | Common:1; Rare:47 | ||||
| chr2:218568296-218568702 | Common:4; Rare:103 | ||||
| chr2:218568746-218568939 | Common:1; Rare:51 | ||||
| chr2:218569266-218569371 | Common:2; Rare:24 | ||||
| chr2:218659600-218659733 | Rare:32 | ||||
| chr2:218671974-218672339 | Common:2; Rare:90 | ||||
| chr2:219176922-219177073 | Common:4; Rare:46 | ||||
| chr2:219206683-219206916 | Rare:86 | ||||
| chr2:219229313-219229419 | Rare:34 | ||||
| chr2:219229577-219229885 | Common:2; Rare:90 | ||||
| chr2:219245391-219245568 | Common:1; Rare:53 | ||||
| chr2:219279139-219279546 | Common:3; Rare:121; Clinvar (benign):1 | ||||
| chr2:219419863-219420151 | Common:1; Rare:59; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr2:219498664-219498944 | Common:2; Rare:63 |