Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:81221354-81221649 | Common:1; Rare:95 | ||||
chr14:81435820-81435843 | Rare:3 | ||||
chr14:81436353-81436586 | Common:3; Rare:80 | ||||
chr14:85530018-85530199 | Common:1; Rare:40 | ||||
chr14:87992988-87993301 | Common:4; Rare:149; Clinvar:14; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
chr14:88562908-88563122 | Rare:101 | ||||
chr14:88824396-88824716 | Common:2; Rare:93; Clinvar:3; Clinvar (benign):1 | ||||
chr14:89619097-89619289 | Common:1; Rare:68 | ||||
chr14:89954694-89954950 | Rare:71 | ||||
chr14:90256254-90256607 | Common:3; Rare:82 | ||||
chr14:90331894-90332188 | Common:1; Rare:87 | ||||
chr14:90396813-90397151 | Common:7; Rare:174 | ||||
chr14:91060125-91060393 | Common:3; Rare:96 | ||||
chr14:91060553-91060704 | Rare:54 | ||||
chr14:91114010-91114175 | Common:1; Rare:53 |