Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45792761-45793079 | Common:2; Rare:83 | ||||
chr19:45863056-45863420 | Common:5; Rare:116 | ||||
chr19:45864153-45864536 | Common:3; Rare:93 | ||||
chr19:45995166-45995501 | Rare:129 | ||||
chr19:46296850-46297072 | Common:4; Rare:84 | ||||
chr19:46346910-46347199 | Common:3; Rare:104 | ||||
chr19:46413515-46413749 | Common:1; Rare:78 | ||||
chr19:46600913-46601432 | Common:6; Rare:178; Clinvar (benign):3 | ||||
chr19:46745845-46746066 | Common:3; Rare:44 | ||||
chr19:46746155-46746381 | Common:1; Rare:41 | ||||
chr19:46746418-46746548 | Common:2; Rare:48 | ||||
chr19:46746785-46746904 | Rare:15 | ||||
chr19:46746958-46747008 | Rare:4 | ||||
chr19:46787255-46787391 | Rare:31 | ||||
chr19:46787403-46787534 | Rare:42 |