Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:92121667-92121975 | Common:4; Rare:103 | ||||
chr14:93184851-93185004 | Rare:49 | ||||
chr14:93207024-93207281 | Common:2; Rare:126 | ||||
chr14:94081154-94081305 | Common:2; Rare:52 | ||||
chr14:95157424-95157685 | Common:4; Rare:93 | ||||
chr14:95534604-95534670 | Rare:18 | ||||
chr14:96363369-96363550 | Common:1; Rare:60 | ||||
chr14:96502232-96502442 | Common:1; Rare:82 | ||||
chr14:99480792-99481128 | Common:1; Rare:117 | ||||
chr14:100376264-100376472 | Common:3; Rare:70 | ||||
chr14:102139309-102139430 | Rare:54 | ||||
chr14:102139656-102139916 | Rare:90 | ||||
chr14:102362847-102363075 | Rare:109 | ||||
chr14:103333900-103334204 | Common:3; Rare:123 | ||||
chr14:103562624-103563019 | Common:6; Rare:143; Clinvar (benign):2 |