| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:30795618-30795732 | Common:1; Rare:28 | ||||
| chr12:46524286-46524469 | Common:1; Rare:26 | ||||
| chr12:52147331-52147569 | Common:2; Rare:55 | ||||
| chr12:87820919-87821054 | Common:1; Rare:28 | ||||
| chr12:93773260-93773412 | Rare:28 | ||||
| chr12:123270269-123270550 | Common:3; Rare:83 | ||||
| chr13:52194402-52194642 | Common:2; Rare:56 | ||||
| chr13:109265323-109265419 | Common:2; Rare:27 | ||||
| chr13:110308524-110308622 | Common:1; Rare:15 | ||||
| chr14:49633956-49634064 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49862674-49863028 | Common:1; Rare:164 | ||||
| chr14:100825921-100826123 | Rare:29 | ||||
| chr15:28589231-28589509 | Common:1; Rare:9 | ||||
| chr15:73927695-73927851 | Common:1; Rare:46 | ||||
| chr16:56617369-56617524 | Common:3; Rare:33 |