Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:77376966-77377415 | Common:5; Rare:130 | ||||
chr14:77457529-77457886 | Common:2; Rare:108 | ||||
chr14:77616755-77617083 | Common:1; Rare:72; Clinvar (benign):2 | ||||
chr14:77707987-77708133 | Common:1; Rare:76 | ||||
chr14:77761126-77761266 | Rare:53 | ||||
chr14:79279126-79279412 | Common:3; Rare:65 | ||||
chr14:79280376-79280527 | Rare:44 | ||||
chr14:81220710-81221069 | Common:3; Rare:141 | ||||
chr14:81221274-81221543 | Common:1; Rare:83 | ||||
chr14:81436421-81436586 | Common:1; Rare:63 | ||||
chr14:85530024-85530190 | Common:1; Rare:36 | ||||
chr14:87993010-87993298 | Common:4; Rare:137; Clinvar:13; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
chr14:88551455-88551609 | Common:2; Rare:34 | ||||
chr14:88562907-88563086 | Rare:83 | ||||
chr14:88824331-88824716 | Common:2; Rare:110; Clinvar:3; Clinvar (benign):1 |