Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:191014124-191014333 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191677856-191678161 | Common:4; Rare:86 | ||||
chr2:192194896-192195044 | Rare:30 | ||||
chr2:196799621-196799782 | Common:1; Rare:44 | ||||
chr2:197434973-197435192 | Rare:75 | ||||
chr2:197453149-197453556 | Rare:137 | ||||
chr2:197499807-197500422 | Common:1; Rare:237; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197515829-197516087 | Common:2; Rare:95 | ||||
chr2:199911120-199911428 | Rare:106 | ||||
chr2:200609087-200609222 | Rare:34 | ||||
chr2:200811403-200811589 | Common:1; Rare:65 | ||||
chr2:200811817-200811964 | Rare:62 | ||||
chr2:200864229-200864252 | Rare:6 | ||||
chr2:200864629-200864791 | Rare:65 | ||||
chr2:200889011-200889439 | Common:3; Rare:140 |