Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61076830-61077310 | Common:10; Rare:220 | ||||
chr1:61082059-61082298 | Rare:115 | ||||
chr1:61082337-61082818 | Common:3; Rare:207 | ||||
chr1:61725087-61725232 | Common:1; Rare:139 | ||||
chr1:61742339-61742534 | Rare:56 | ||||
chr1:62319330-62319547 | Common:2; Rare:43 | ||||
chr1:62436247-62436678 | Common:5; Rare:149 | ||||
chr1:62436723-62437130 | Common:1; Rare:110 | ||||
chr1:62687170-62687948 | Common:1; Rare:224 | ||||
chr1:62688265-62688553 | Common:2; Rare:213 | ||||
chr1:62784062-62784191 | Rare:102 | ||||
chr1:63367454-63367700 | Rare:141; Clinvar (benign):2 | ||||
chr1:63523149-63523581 | Common:6; Rare:222 | ||||
chr1:63593188-63593564 | Rare:247; Clinvar (benign):4 | ||||
chr1:63773891-63774189 | Rare:82 |