Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:89619097-89619260 | Common:1; Rare:58 | ||||
chr14:89955764-89955980 | Common:10; Rare:74; Clinvar:3; Clinvar (benign):1 | ||||
chr14:90396870-90397192 | Common:5; Rare:152 | ||||
chr14:91113943-91114090 | Rare:40 | ||||
chr14:91114301-91114395 | Rare:15 | ||||
chr14:91510183-91510652 | Common:1; Rare:161 | ||||
chr14:92040028-92040192 | Common:2; Rare:44; Clinvar (benign):1 | ||||
chr14:92121658-92121985 | Common:4; Rare:109 | ||||
chr14:92651355-92651632 | Common:2; Rare:67 | ||||
chr14:93115244-93115607 | Common:3; Rare:118 | ||||
chr14:93184842-93185013 | Rare:57 | ||||
chr14:93207055-93207289 | Common:2; Rare:116 | ||||
chr14:93333011-93333186 | Common:1; Rare:64 | ||||
chr14:94081130-94081404 | Common:5; Rare:82 | ||||
chr14:95157348-95157693 | Common:4; Rare:117; Clinvar:1 |