Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151198412-151198614 | Common:1; Rare:73 | ||||
chr1:151254627-151254791 | Rare:42 | ||||
chr1:151281500-151281633 | Common:4; Rare:38 | ||||
chr1:151281884-151282319 | Rare:121 | ||||
chr1:151282370-151282519 | Common:1; Rare:51 | ||||
chr1:151327628-151327841 | Common:2; Rare:43 | ||||
chr1:151346843-151347038 | Rare:55 | ||||
chr1:151347182-151347428 | Rare:58 | ||||
chr1:151399484-151399786 | Common:4; Rare:97; Clinvar (pathogenic):2 | ||||
chr1:151459211-151459526 | Common:2; Rare:127 | ||||
chr1:151763423-151763576 | Common:2; Rare:61 | ||||
chr1:151790426-151790871 | Common:3; Rare:108 | ||||
chr1:151909174-151909709 | Common:4; Rare:176 | ||||
chr1:151909837-151910142 | Common:2; Rare:69 | ||||
chr1:151992571-151992777 | Common:1; Rare:47 |