| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73780041-73780166 | Rare:73 | ||||
| chr2:73828804-73829054 | Common:2; Rare:60 | ||||
| chr2:74147821-74148140 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:74178784-74179057 | Common:3; Rare:78 | ||||
| chr2:74198443-74198664 | Rare:98 | ||||
| chr2:74421629-74421759 | Rare:42 | ||||
| chr2:74440523-74440646 | Rare:39 | ||||
| chr2:74441854-74441997 | Common:1; Rare:33 | ||||
| chr2:74465336-74465511 | Common:1; Rare:48; Clinvar:1 | ||||
| chr2:74482937-74483119 | Common:1; Rare:71 | ||||
| chr2:74507263-74507448 | Rare:48 | ||||
| chr2:74507653-74507801 | Rare:32 | ||||
| chr2:74527471-74527742 | Common:1; Rare:92 | ||||
| chr2:74529360-74530036 | Common:2; Rare:233; Clinvar:5; Clinvar (benign):3 | ||||
| chr2:74530281-74530616 | Common:4; Rare:112; Clinvar:3; Clinvar (benign):2 |