Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:66925446-66925680 | Common:1; Rare:93 | ||||
chr8:66926423-66926477 | Rare:14 | ||||
chr8:67158318-67158594 | Rare:75; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr8:67163092-67163143 | Rare:8 | ||||
chr8:70149182-70149452 | Common:2; Rare:50 | ||||
chr8:70225279-70225476 | Common:1; Rare:55 | ||||
chr8:70586960-70587168 | Rare:36 | ||||
chr8:73322692-73322961 | Rare:62 | ||||
chr8:75223765-75223862 | Common:1; Rare:16 | ||||
chr8:79793789-79793840 | Rare:10 | ||||
chr8:80039512-80039755 | Common:3; Rare:34 | ||||
chr8:86451259-86451279 | Common:1; Rare:5 | ||||
chr8:89246310-89246633 | Common:1; Rare:56 | ||||
chr8:89246939-89247024 | Common:1; Rare:19 | ||||
chr8:89340117-89340170 | Common:1; Rare:11 |