Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:101809686-101809871 | Rare:36 | ||||
chr14:102362866-102363068 | Rare:95 | ||||
chr14:103562624-103562996 | Common:5; Rare:132; Clinvar (benign):1 | ||||
chr15:34101843-34102083 | Common:1; Rare:48 | ||||
chr15:34795534-34795676 | Common:1; Rare:24; Clinvar:2; Clinvar (benign):1 | ||||
chr15:40039112-40039329 | Rare:94 | ||||
chr15:40807455-40807751 | Common:3; Rare:97 | ||||
chr15:42273416-42273527 | Rare:40 | ||||
chr15:42548774-42548868 | Common:1; Rare:54 | ||||
chr15:43510688-43510954 | Rare:85 | ||||
chr15:44427472-44427643 | Rare:44 | ||||
chr15:45634929-45635079 | Rare:44 | ||||
chr15:49155574-49155783 | Common:1; Rare:72 | ||||
chr15:49620810-49621083 | Common:6; Rare:104 | ||||
chr15:55408261-55408667 | Common:4; Rare:87 |