Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61742182-61742496 | Rare:71 | ||||
chr1:62436239-62436356 | Common:2; Rare:39 | ||||
chr1:62688269-62688533 | Common:1; Rare:102 | ||||
chr1:62784069-62784180 | Rare:44 | ||||
chr1:63523165-63523592 | Common:3; Rare:113 | ||||
chr1:63593186-63593503 | Rare:116; Clinvar (benign):1 | ||||
chr1:63593654-63593678 | Rare:10; Clinvar (pathogenic):1 | ||||
chr1:65147221-65147653 | Common:1; Rare:105 | ||||
chr1:65148060-65148305 | Common:3; Rare:52 | ||||
chr1:65148686-65149099 | Common:6; Rare:120 | ||||
chr1:65254338-65254547 | Common:2; Rare:77 | ||||
chr1:66533869-66534165 | Common:2; Rare:75 | ||||
chr1:66752346-66752533 | Rare:39 | ||||
chr1:66924784-66925024 | Common:1; Rare:107 | ||||
chr1:66925187-66925518 | Common:2; Rare:103 |