| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75002741-75002967 | Common:1; Rare:68; Clinvar:2 | ||||
| chr14:75069493-75069680 | Common:1; Rare:43 | ||||
| chr14:75127001-75127116 | Rare:38 | ||||
| chr14:75660825-75660991 | Rare:42 | ||||
| chr14:75661175-75661334 | Common:2; Rare:43 | ||||
| chr14:77377082-77377410 | Common:1; Rare:89 | ||||
| chr14:77457546-77458129 | Common:2; Rare:161 | ||||
| chr14:77707991-77708152 | Common:2; Rare:87 | ||||
| chr14:81220871-81221046 | Common:1; Rare:85 | ||||
| chr14:85530033-85530184 | Common:1; Rare:34 | ||||
| chr14:89349979-89350312 | Rare:66 | ||||
| chr14:90331921-90332181 | Common:1; Rare:69 | ||||
| chr14:91836421-91836744 | Common:12; Rare:61 | ||||
| chr14:91946947-91947083 | Common:1; Rare:15 | ||||
| chr14:92040019-92040192 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 |