Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:41332263-41332393 | Common:1; Rare:64 | ||||
chr15:41332494-41332946 | Common:2; Rare:189 | ||||
chr15:41333102-41333266 | Common:1; Rare:24 | ||||
chr15:41333269-41333617 | Common:1; Rare:78 | ||||
chr15:41402269-41402793 | Common:5; Rare:152; Clinvar:3; Clinvar (benign):1 | ||||
chr15:41416723-41416804 | Rare:13 | ||||
chr15:41416896-41417223 | Common:4; Rare:136 | ||||
chr15:41493199-41493392 | Rare:45 | ||||
chr15:41493557-41493875 | Rare:81 | ||||
chr15:41544021-41544403 | Common:3; Rare:118 | ||||
chr15:41621160-41621262 | Common:1; Rare:28 | ||||
chr15:41621414-41621824 | Common:1; Rare:103 | ||||
chr15:41660176-41660570 | Rare:102 | ||||
chr15:41660645-41660821 | Rare:56 | ||||
chr15:41660866-41660954 | Common:2; Rare:30 |