| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49633866-49634079 | Common:1; Rare:78; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr14:49789221-49789532 | Rare:85 | ||||
| chr14:49789533-49789673 | Rare:30 | ||||
| chr14:49862639-49863039 | Common:1; Rare:182 | ||||
| chr14:49868119-49868367 | Common:1; Rare:52 | ||||
| chr14:49977166-49977218 | Rare:8 | ||||
| chr14:50003413-50003524 | Rare:32 | ||||
| chr14:50362645-50362880 | Common:2; Rare:52 | ||||
| chr14:52315362-52315671 | Rare:60 | ||||
| chr14:54870239-54870367 | Common:1; Rare:19 | ||||
| chr14:55275746-55276063 | Common:5; Rare:64 | ||||
| chr14:56120477-56120509 | Rare:9 | ||||
| chr14:56310753-56311004 | Common:2; Rare:45 | ||||
| chr14:58266482-58266591 | Common:1; Rare:17 | ||||
| chr14:58266725-58266980 | Rare:47 |