| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74881755-74881982 | Common:1; Rare:103 | ||||
| chr14:74955584-74955712 | Common:2; Rare:53 | ||||
| chr14:75002743-75002961 | Common:1; Rare:62; Clinvar:2 | ||||
| chr14:75051418-75051526 | Common:2; Rare:31; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:75069375-75069652 | Common:2; Rare:124 | ||||
| chr14:75126969-75127144 | Common:1; Rare:118 | ||||
| chr14:75176570-75176869 | Common:1; Rare:80 | ||||
| chr14:75427730-75428120 | Rare:98 | ||||
| chr14:75660794-75661087 | Common:1; Rare:143 | ||||
| chr14:75661114-75661400 | Common:7; Rare:112 | ||||
| chr14:76151731-76151984 | Rare:152 | ||||
| chr14:77028602-77028944 | Rare:161 | ||||
| chr14:77097850-77098370 | Rare:273 | ||||
| chr14:77320838-77321114 | Rare:151; Clinvar:2 | ||||
| chr14:77321200-77321510 | Common:14; Rare:303 |