Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234610157-234610320 | Common:2; Rare:69 | ||||
chr10:5524835-5524978 | Rare:41 | ||||
chr10:24953702-24953891 | Rare:29 | ||||
chr10:29409487-29409599 | Common:1; Rare:32 | ||||
chr10:32919886-32920386 | Common:3; Rare:127 | ||||
chr10:46786829-46786876 | Rare:2 | ||||
chr10:47553490-47553598 | Rare:12 | ||||
chr10:68600450-68600500 | Rare:13 | ||||
chr10:73247197-73247339 | Rare:81 | ||||
chr10:73730462-73730595 | Rare:35 | ||||
chr10:79826331-79826419 | Common:2; Rare:31 | ||||
chr10:86955615-86955771 | Rare:25 | ||||
chr10:86971209-86971480 | Common:2; Rare:89 | ||||
chr10:87342283-87342417 | Common:3; Rare:41 | ||||
chr10:88948916-88949117 | Rare:43; Clinvar:1; Clinvar (pathogenic):1 |