Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:12019263-12019528 | Common:5; Rare:91 | ||||
chr1:15526623-15526905 | Common:2; Rare:92 | ||||
chr1:15756540-15756651 | Rare:31 | ||||
chr1:15758734-15758810 | Common:1; Rare:16 | ||||
chr1:16352420-16352606 | Common:3; Rare:99 | ||||
chr1:16613486-16613645 | Common:1 | ||||
chr1:17053997-17054320 | Common:3; Rare:96; Clinvar:5; Clinvar (benign):7 | ||||
chr1:19210264-19210417 | Rare:60 | ||||
chr1:19251512-19251899 | Common:8; Rare:135 | ||||
chr1:19312137-19312306 | Common:5; Rare:77 | ||||
chr1:19485449-19485762 | Rare:116 | ||||
chr1:19596854-19597064 | Common:2; Rare:93 | ||||
chr1:20486188-20486369 | Rare:41 | ||||
chr1:20508097-20508187 | Common:2; Rare:33 | ||||
chr1:20661457-20661718 | Common:1; Rare:82; Clinvar:2 |