| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:89619111-89619315 | Common:1; Rare:70 | ||||
| chr14:89954504-89954593 | Rare:32 | ||||
| chr14:89954633-89954975 | Common:1; Rare:105 | ||||
| chr14:90256481-90256600 | Common:1; Rare:40 | ||||
| chr14:90331908-90332203 | Common:1; Rare:85 | ||||
| chr14:90396870-90397151 | Common:5; Rare:142 | ||||
| chr14:91060132-91060354 | Common:2; Rare:71 | ||||
| chr14:91060546-91060972 | Common:3; Rare:119 | ||||
| chr14:91114002-91114090 | Rare:26 | ||||
| chr14:91114283-91114402 | Rare:20 | ||||
| chr14:91510268-91510637 | Common:1; Rare:119 | ||||
| chr14:92040008-92040192 | Common:3; Rare:57; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:92106532-92106771 | Common:2; Rare:76 | ||||
| chr14:92121647-92122021 | Common:5; Rare:129 | ||||
| chr14:92748604-92748812 | Rare:58 |