| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23057487-23057732 | Common:10; Rare:124 | ||||
| chr14:23094580-23094791 | Common:1; Rare:72 | ||||
| chr14:23095080-23095609 | Common:6; Rare:455 | ||||
| chr14:23285982-23286450 | Common:2; Rare:207 | ||||
| chr14:23301050-23301480 | Common:6; Rare:144 | ||||
| chr14:23301510-23302160 | Common:2; Rare:204 | ||||
| chr14:23302385-23302520 | Rare:83 | ||||
| chr14:23306696-23306994 | Common:2; Rare:111 | ||||
| chr14:23320870-23321070 | Common:4; Rare:77 | ||||
| chr14:23321197-23321551 | Common:2; Rare:224; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr14:23321610-23322010 | Common:5; Rare:202; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:23469270-23469753 | Common:8; Rare:214 | ||||
| chr14:23551560-23551960 | Rare:196 | ||||
| chr14:23555874-23556191 | Common:3; Rare:136 | ||||
| chr14:23556137-23556417 | Common:4; Rare:96 |