Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:14122133-14122247 | Common:3; Rare:43 | ||||
chr8:15585500-15585760 | Common:4; Rare:73 | ||||
chr8:17232429-17232670 | Common:1; Rare:47 | ||||
chr8:17284297-17284580 | Common:1; Rare:73; Clinvar (benign):1 | ||||
chr8:20268239-20268329 | Rare:15 | ||||
chr8:20435310-20435616 | Common:3; Rare:72 | ||||
chr8:22259669-22259689 | Rare:2 | ||||
chr8:23961480-23961547 | Common:1; Rare:9 | ||||
chr8:23961602-23961641 | Rare:7 | ||||
chr8:24609595-24609763 | Common:2; Rare:20 | ||||
chr8:24941949-24942024 | Common:1; Rare:15 | ||||
chr8:24955171-24955484 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
chr8:25510974-25511046 | Common:1; Rare:14 | ||||
chr8:30033621-30033696 | Rare:14 | ||||
chr8:30035317-30035564 | Common:5; Rare:42 |