Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:77246991-77247279 | Rare:52 | ||||
chr10:77925394-77925697 | Rare:48 | ||||
chr10:79826324-79826908 | Common:4; Rare:178 | ||||
chr10:86755760-86755871 | Rare:26 | ||||
chr10:86757267-86757306 | Rare:8 | ||||
chr10:86955645-86955786 | Rare:24 | ||||
chr10:86970916-86971067 | Common:3; Rare:30 | ||||
chr10:86971168-86971196 | Rare:7 | ||||
chr10:86971202-86971379 | Rare:56 | ||||
chr10:87342260-87342920 | Common:6; Rare:202 | ||||
chr10:88939491-88939961 | Common:2; Rare:81; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr10:88948800-88949117 | Rare:61; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr10:95349590-95349823 | Common:3; Rare:36 | ||||
chr10:95422191-95422435 | Common:1; Rare:49 | ||||
chr10:95480174-95480443 | Common:2; Rare:52 |