Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:46786803-46786876 | Rare:5 | ||||
chr10:47553472-47553605 | Rare:15 | ||||
chr10:50623360-50623475 | Common:1; Rare:25 | ||||
chr10:61903029-61903360 | Common:1; Rare:88 | ||||
chr10:63464932-63465197 | Common:1; Rare:76 | ||||
chr10:69421927-69422161 | Common:2; Rare:43 | ||||
chr10:71772256-71772434 | Common:1; Rare:41 | ||||
chr10:71965260-71965356 | Common:1; Rare:23 | ||||
chr10:73247247-73247382 | Rare:74 | ||||
chr10:73730452-73730591 | Common:1; Rare:37 | ||||
chr10:74070647-74071083 | Common:1; Rare:85; Clinvar:2; Clinvar (benign):8 | ||||
chr10:74088973-74089349 | Common:1; Rare:74; Clinvar:5; Clinvar (benign):2 | ||||
chr10:74097544-74097566 | Rare:5 | ||||
chr10:74114719-74114894 | Rare:32; Clinvar:2; Clinvar (benign):2 | ||||
chr10:76970609-76970715 | Common:1; Rare:21 |