Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:96502232-96502442 | Common:1; Rare:82 | ||||
chr14:100376269-100376485 | Common:3; Rare:73 | ||||
chr14:102139678-102139897 | Rare:69 | ||||
chr14:102362866-102363075 | Rare:98 | ||||
chr14:103562624-103562996 | Common:5; Rare:132; Clinvar (benign):1 | ||||
chr14:105021031-105021374 | Common:1; Rare:122 | ||||
chr15:22838356-22838673 | Common:3; Rare:106 | ||||
chr15:30903692-30903912 | Common:1; Rare:55 | ||||
chr15:34988262-34988409 | Common:1; Rare:61 | ||||
chr15:35546143-35546256 | Common:1; Rare:39 | ||||
chr15:39580818-39581086 | Common:1; Rare:72 | ||||
chr15:39933956-39934211 | Common:4; Rare:91 | ||||
chr15:40039103-40039329 | Rare:96 | ||||
chr15:40340916-40341020 | Common:1; Rare:36 | ||||
chr15:40405594-40405811 | Common:2; Rare:59; Clinvar (benign):3 |