| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:38932551-38932740 | Rare:41 | ||||
| chr14:39036680-39036980 | Common:2; Rare:44 | ||||
| chr14:39203730-39204010 | Common:4; Rare:74 | ||||
| chr14:49633899-49634138 | Common:2; Rare:178; Clinvar:20; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
| chr14:49634270-49634580 | Common:2; Rare:229; Clinvar:19; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:49770370-49770650 | Common:1; Rare:84 | ||||
| chr14:49862780-49863070 | Rare:194 | ||||
| chr14:50001269-50001410 | Common:4; Rare:50 | ||||
| chr14:50003240-50003700 | Common:6; Rare:241 | ||||
| chr14:50059810-50060080 | Rare:46 | ||||
| chr14:53613720-53614320 | Common:2; Rare:176 | ||||
| chr14:54102090-54102400 | Common:6; Rare:62 | ||||
| chr14:54133880-54134260 | Common:11; Rare:86 | ||||
| chr14:54135720-54136330 | Common:9; Rare:182 | ||||
| chr14:54136850-54137240 | Common:2; Rare:148 |