Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16613486-16613665 | Common:1 | ||||
chr1:17439747-17439880 | Rare:49 | ||||
chr1:19210211-19210515 | Rare:104 | ||||
chr1:19251512-19251852 | Common:6; Rare:111 | ||||
chr1:19311957-19312352 | Common:8; Rare:175 | ||||
chr1:19485446-19485736 | Rare:97 | ||||
chr1:19596742-19597096 | Common:3; Rare:130 | ||||
chr1:19799864-19800218 | Common:5; Rare:95 | ||||
chr1:19979547-19979875 | Common:2; Rare:61 | ||||
chr1:20028212-20028600 | Common:2; Rare:94 | ||||
chr1:20185875-20186138 | Common:1; Rare:84 | ||||
chr1:20508041-20508200 | Common:2; Rare:59 | ||||
chr1:20661346-20661716 | Common:3; Rare:133; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786573-20786870 | Rare:110 | ||||
chr1:20787219-20787470 | Rare:119 |