Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:149551364-149551638 | Rare:63 | ||||
chr5:149960597-149960919 | Rare:107; Clinvar:7 | ||||
chr5:150486183-150486313 | Common:1; Rare:26 | ||||
chr5:151020264-151020566 | Common:3; Rare:66 | ||||
chr5:151080946-151081154 | Common:1; Rare:70 | ||||
chr5:151531875-151532230 | Common:1; Rare:96 | ||||
chr5:154038876-154038989 | Common:1; Rare:37 | ||||
chr5:154793669-154793952 | Common:1; Rare:108 | ||||
chr5:154858449-154858698 | Common:1; Rare:80 | ||||
chr5:157460086-157460269 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
chr5:159263236-159263326 | Common:1; Rare:28 | ||||
chr5:160419049-160419171 | Common:2; Rare:38 | ||||
chr5:163437316-163437641 | Rare:101 | ||||
chr5:172006616-172006942 | Common:1; Rare:71 | ||||
chr5:172770579-172770935 | Common:3; Rare:94 |