Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:173168712-173168864 | Common:3; Rare:57 | ||||
chr4:173334245-173334656 | Rare:114 | ||||
chr4:173369748-173369956 | Common:1; Rare:72 | ||||
chr4:173370015-173370274 | Rare:60 | ||||
chr4:173370659-173371036 | Common:2; Rare:93 | ||||
chr4:173371078-173371395 | Common:4; Rare:107 | ||||
chr4:173529336-173529623 | Rare:66 | ||||
chr4:173530083-173530544 | Common:3; Rare:91 | ||||
chr4:174283417-174283977 | Common:2; Rare:101 | ||||
chr4:174522272-174522617 | Common:1; Rare:108; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr4:176319727-176320085 | Common:5; Rare:119 | ||||
chr4:177442377-177442526 | Rare:89; Clinvar:2 | ||||
chr4:182144418-182144734 | Common:3; Rare:102 | ||||
chr4:182917319-182917554 | Common:4; Rare:80 | ||||
chr4:183444309-183444727 | Common:2; Rare:179 |