Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58326875-58327043 | Common:1; Rare:38 | ||||
chr19:58327263-58327347 | Rare:18 | ||||
chr19:58347600-58347806 | Common:8; Rare:96 | ||||
chr19:58408431-58408749 | Common:4; Rare:99 | ||||
chr19:58499202-58499560 | Common:2; Rare:120; Clinvar:5; Clinvar (benign):1 | ||||
chr19:58519750-58519882 | Rare:28 | ||||
chr19:58558317-58558681 | Rare:118 | ||||
chr19:58558931-58559127 | Common:1; Rare:60 | ||||
chr2:264561-264989 | Common:4; Rare:164 | ||||
chr2:3519501-3519667 | Common:1; Rare:42 | ||||
chr2:3558216-3558688 | Common:6; Rare:178 | ||||
chr2:3575111-3575376 | Common:2; Rare:80; Clinvar:3; Clinvar (benign):6 | ||||
chr2:9423155-9423703 | Common:1; Rare:149 | ||||
chr2:9555671-9555937 | Common:2; Rare:91 | ||||
chr2:10302715-10302935 | Common:4; Rare:76 |