| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:41605287-41605401 | Common:2; Rare:23 | ||||
| chr14:49633902-49634087 | Common:1; Rare:78; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:49778397-49778429 | Rare:8 | ||||
| chr14:49789497-49789789 | Rare:64 | ||||
| chr14:49799523-49799559 | Rare:9 | ||||
| chr14:49813998-49814251 | Common:2; Rare:63 | ||||
| chr14:49853722-49853741 | Rare:6 | ||||
| chr14:49853800-49853919 | Rare:30 | ||||
| chr14:49862396-49862592 | Rare:58 | ||||
| chr14:49862624-49862999 | Common:1; Rare:171 | ||||
| chr14:49868124-49868453 | Common:3; Rare:73 | ||||
| chr14:52001568-52001860 | Common:1; Rare:62 | ||||
| chr14:52315335-52315767 | Common:1; Rare:92 | ||||
| chr14:52954661-52954867 | Common:1; Rare:37 | ||||
| chr14:53217831-53217947 | Common:2; Rare:27 |