| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197499785-197499993 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197500106-197500446 | Common:1; Rare:143 | ||||
| chr2:197515782-197516107 | Common:2; Rare:112 | ||||
| chr2:199911104-199911443 | Rare:118 | ||||
| chr2:200306432-200306587 | Common:2; Rare:36 | ||||
| chr2:200509907-200510263 | Common:2; Rare:121 | ||||
| chr2:200609094-200609255 | Rare:37 | ||||
| chr2:200811362-200811596 | Common:1; Rare:78 | ||||
| chr2:200812300-200812449 | Common:2; Rare:51 | ||||
| chr2:200864192-200864252 | Rare:21 | ||||
| chr2:200864585-200864788 | Common:1; Rare:77 | ||||
| chr2:200888974-200889479 | Common:3; Rare:159 | ||||
| chr2:200963615-200963838 | Common:1; Rare:59 | ||||
| chr2:201071592-201072047 | Rare:99 | ||||
| chr2:201257972-201258348 | Common:3; Rare:88; Clinvar (benign):2 |