| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23409592-23409810 | Common:2; Rare:39 | ||||
| chr14:23415349-23415849 | Common:1; Rare:153; Clinvar:23; Clinvar (benign):16; Clinvar (pathogenic):5 | ||||
| chr14:23425693-23426088 | Common:1; Rare:98; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):9 | ||||
| chr14:23428953-23429351 | Rare:97; Clinvar:7; Clinvar (benign):13; Clinvar (pathogenic):6 | ||||
| chr14:23431416-23431691 | Common:1; Rare:68; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr14:23432477-23432796 | Rare:78; Clinvar:8; Clinvar (benign):14; Clinvar (pathogenic):4 | ||||
| chr14:32203476-32203686 | Common:3; Rare:86 | ||||
| chr14:32418051-32418420 | Common:1; Rare:58 | ||||
| chr14:49633866-49634070 | Common:1; Rare:74; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:49862645-49862994 | Common:1; Rare:165 | ||||
| chr14:52001756-52001856 | Rare:26 | ||||
| chr14:77343820-77343874 | Common:1; Rare:14 | ||||
| chr14:81170391-81170506 | Rare:36 | ||||
| chr14:93986945-93987225 | Common:1; Rare:59 | ||||
| chr14:95516616-95516784 | Common:2; Rare:40 |