Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:74713042-74713218 | Rare:101 | ||||
chr14:74809950-74810263 | Rare:65 | ||||
chr14:74881778-74881990 | Common:1; Rare:99 | ||||
chr14:74955402-74955504 | Common:1; Rare:24 | ||||
chr14:75002741-75002982 | Common:1; Rare:79; Clinvar:2 | ||||
chr14:75051416-75051525 | Common:2; Rare:31; Clinvar:3; Clinvar (benign):2 | ||||
chr14:75069355-75069756 | Common:2; Rare:98 | ||||
chr14:75126878-75127128 | Rare:83 | ||||
chr14:75278945-75279123 | Rare:55 | ||||
chr14:75427671-75427759 | Rare:19 | ||||
chr14:75660789-75661003 | Rare:55 | ||||
chr14:75661163-75661383 | Common:3; Rare:63 | ||||
chr14:77028684-77028803 | Rare:39 | ||||
chr14:77097989-77098361 | Rare:120 | ||||
chr14:77320832-77321108 | Rare:86; Clinvar:1 |