Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:148020694-148021098 | Common:2; Rare:93; Clinvar (benign):2 | ||||
chr2:148021502-148021675 | Rare:35 | ||||
chr2:159712416-159712538 | Common:2; Rare:52 | ||||
chr2:162318650-162318774 | Rare:22 | ||||
chr2:171433957-171434275 | Common:2; Rare:80 | ||||
chr2:172427274-172427725 | Common:10; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
chr2:174395642-174395812 | Common:1; Rare:58 | ||||
chr2:176188507-176188729 | Common:2; Rare:90 | ||||
chr2:177392677-177392808 | Rare:35; Clinvar:1 | ||||
chr2:178451129-178451381 | Common:5; Rare:70; Clinvar:3; Clinvar (benign):3 | ||||
chr2:186486048-186486367 | Common:3; Rare:96 | ||||
chr2:187554267-187554579 | Common:2; Rare:59 | ||||
chr2:189441148-189441529 | Common:2; Rare:124 | ||||
chr2:189783942-189784131 | Common:4; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
chr2:191245207-191245463 | Common:2; Rare:85 |