Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:183023097-183023256 | Common:4; Rare:44 | ||||
chr1:183023933-183024092 | Rare:42 | ||||
chr1:183472308-183472538 | Common:2; Rare:79 | ||||
chr1:183635645-183636146 | Common:5; Rare:137 | ||||
chr1:185045269-185045632 | Common:2; Rare:123 | ||||
chr1:185156701-185156722 | Rare:13 | ||||
chr1:185156723-185157303 | Common:3; Rare:167 | ||||
chr1:185317214-185317430 | Common:1; Rare:67 | ||||
chr1:186375111-186375482 | Rare:104 | ||||
chr1:186375667-186375920 | Common:1; Rare:65 | ||||
chr1:192808794-192809138 | Common:4; Rare:151 | ||||
chr1:193059330-193059482 | Rare:63 | ||||
chr1:193059485-193059746 | Common:1; Rare:129 | ||||
chr1:193105378-193105523 | Common:3; Rare:60 | ||||
chr1:193121764-193122192 | Common:2; Rare:148; Clinvar:5; Clinvar (benign):3 |