| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:45253048-45253408 | Common:1; Rare:103 | ||||
| chr14:45253481-45253678 | Common:2; Rare:76 | ||||
| chr14:45254032-45254112 | Rare:16 | ||||
| chr14:49585952-49586158 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
| chr14:49586356-49586605 | Common:1; Rare:109 | ||||
| chr14:49598499-49598788 | Common:3; Rare:118 | ||||
| chr14:49598814-49599093 | Common:1; Rare:98 | ||||
| chr14:49599107-49599338 | Rare:70 | ||||
| chr14:49620138-49620374 | Rare:58 | ||||
| chr14:49620528-49620922 | Common:4; Rare:142; Clinvar:6; Clinvar (benign):1 | ||||
| chr14:49634684-49634917 | Rare:89; Clinvar:10; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49688090-49688369 | Common:2; Rare:104 | ||||
| chr14:49688462-49688517 | Rare:7 | ||||
| chr14:49692965-49693187 | Common:1; Rare:79 | ||||
| chr14:49693372-49693633 | Common:1; Rare:87 |