Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:211259723-211259980 | Rare:73 | ||||
chr1:211326747-211326867 | Common:3; Rare:29 | ||||
chr1:211675525-211675762 | Rare:50 | ||||
chr1:211830648-211830900 | Common:1; Rare:65 | ||||
chr1:212035507-212035854 | Common:2; Rare:91 | ||||
chr1:212414813-212415023 | Common:3; Rare:64 | ||||
chr1:212608295-212608588 | Common:3; Rare:75 | ||||
chr1:212791701-212791972 | Common:6; Rare:131 | ||||
chr1:212858089-212858453 | Common:5; Rare:98; Clinvar:5; Clinvar (benign):1 | ||||
chr1:212950375-212950604 | Common:2; Rare:56 | ||||
chr1:213015369-213015633 | Rare:71 | ||||
chr1:213015670-213015928 | Rare:84 | ||||
chr1:213051161-213051387 | Common:2; Rare:80 | ||||
chr1:213987694-213987979 | Rare:53 | ||||
chr1:213988214-213988299 | Rare:19 |