| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35336500-35337260 | Common:9; Rare:266 | ||||
| chr14:35337873-35337995 | Rare:29 | ||||
| chr14:35341550-35341950 | Common:8; Rare:137 | ||||
| chr14:35356107-35356250 | Common:1; Rare:33 | ||||
| chr14:35356180-35356390 | Common:2; Rare:27 | ||||
| chr14:38208910-38209135 | Common:2; Rare:96 | ||||
| chr14:39218960-39219360 | Common:6; Rare:135 | ||||
| chr14:39376524-39377193 | Common:6; Rare:183 | ||||
| chr14:39447259-39447659 | Common:4; Rare:104 | ||||
| chr14:49633888-49634137 | Common:2; Rare:173; Clinvar:20; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
| chr14:49634275-49634508 | Common:1; Rare:115; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49861540-49862080 | Common:2; Rare:184 | ||||
| chr14:49862839-49863075 | Rare:155 | ||||
| chr14:49868103-49868367 | Common:2; Rare:111 | ||||
| chr14:50001210-50001510 | Common:5; Rare:94 |