Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111619460-111619938 | Common:2; Rare:134 | ||||
chr1:111739341-111739723 | Common:3; Rare:104 | ||||
chr1:111755402-111755799 | Common:5; Rare:131 | ||||
chr1:112396036-112396268 | Common:1; Rare:71 | ||||
chr1:112619618-112619879 | Common:2; Rare:91 | ||||
chr1:112658758-112659077 | Common:1; Rare:73 | ||||
chr1:112674612-112675013 | Common:2; Rare:95 | ||||
chr1:112715251-112715577 | Rare:95 | ||||
chr1:112956036-112956303 | Common:4; Rare:85; Clinvar:7; Clinvar (benign):3 | ||||
chr1:112956344-112956824 | Common:4; Rare:118; Clinvar:1 | ||||
chr1:113073059-113073287 | Common:1; Rare:92 | ||||
chr1:113390177-113390497 | Common:1; Rare:80 | ||||
chr1:113904761-113905428 | Common:7; Rare:191; Clinvar (benign):2 | ||||
chr1:113929510-113929691 | Common:1; Rare:54 | ||||
chr1:113979301-113979509 | Rare:51 |