Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:67359744-67360018 | Rare:84 | ||||
chr14:67360062-67360389 | Common:4; Rare:83 | ||||
chr14:69398256-69398381 | Rare:51 | ||||
chr14:70416992-70417124 | Rare:40 | ||||
chr14:74493568-74493767 | Common:3; Rare:75; Clinvar (benign):3 | ||||
chr14:74713068-74713217 | Rare:80 | ||||
chr14:75660834-75660962 | Rare:34 | ||||
chr14:77457565-77457845 | Common:1; Rare:87 | ||||
chr14:77708011-77708118 | Rare:47 | ||||
chr14:92121667-92121979 | Common:4; Rare:104 | ||||
chr14:93206994-93207281 | Common:2; Rare:141 | ||||
chr14:94081164-94081341 | Common:3; Rare:59 | ||||
chr14:100375453-100375701 | Common:1; Rare:31 | ||||
chr14:100376286-100376485 | Common:3; Rare:68 | ||||
chr14:102139667-102139914 | Rare:84 |