Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23825356-23825605 | Common:3; Rare:77; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr1:23868221-23868612 | Common:6; Rare:98; Clinvar:2; Clinvar (benign):5 | ||||
chr1:23959005-23959146 | Common:2; Rare:26 | ||||
chr1:23959159-23959451 | Common:2; Rare:65 | ||||
chr1:23959541-23960031 | Common:5; Rare:118 | ||||
chr1:23960043-23960097 | Rare:23 | ||||
chr1:23979842-23979892 | Common:1; Rare:13 | ||||
chr1:23980039-23980115 | Rare:9 | ||||
chr1:23980249-23980627 | Common:1; Rare:113 | ||||
chr1:23980871-23981024 | Common:1; Rare:31 | ||||
chr1:24187230-24187403 | Common:3; Rare:42 | ||||
chr1:24413345-24413417 | Common:1; Rare:12 | ||||
chr1:24413604-24413922 | Common:3; Rare:79 | ||||
chr1:24415422-24415467 | Rare:14 | ||||
chr1:24415479-24415831 | Common:3; Rare:87 |