Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:190319736-190319950 | Common:5; Rare:76; Clinvar (benign):5 | ||||
chr2:190343916-190344031 | Rare:24 | ||||
chr2:190408653-190408816 | Common:3; Rare:38 | ||||
chr2:190648684-190648906 | Common:1; Rare:82 | ||||
chr2:190649454-190649574 | Common:1; Rare:37 | ||||
chr2:190880591-190880886 | Common:4; Rare:102 | ||||
chr2:191014044-191014336 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):3 | ||||
chr2:191678559-191678615 | Rare:25 | ||||
chr2:191847204-191847447 | Rare:36 | ||||
chr2:196799597-196799782 | Common:1; Rare:57 | ||||
chr2:197434975-197435192 | Rare:74 | ||||
chr2:197453240-197453552 | Rare:103 | ||||
chr2:197499820-197500435 | Common:1; Rare:240; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197515780-197516100 | Common:2; Rare:111 | ||||
chr2:200510058-200510199 | Rare:39 |