Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:48301325-48301439 | Common:1; Rare:36 | ||||
chr3:48429993-48430261 | Common:1; Rare:64 | ||||
chr3:48440035-48440312 | Common:1; Rare:103 | ||||
chr3:48556810-48557173 | Common:1; Rare:76 | ||||
chr3:48635447-48635608 | Rare:48 | ||||
chr3:48695399-48695619 | Common:2; Rare:43 | ||||
chr3:48847796-48847973 | Rare:59 | ||||
chr3:48918719-48918905 | Common:2; Rare:100 | ||||
chr3:49007177-49007429 | Common:2; Rare:98 | ||||
chr3:49018552-49018604 | Rare:21 | ||||
chr3:49021503-49021703 | Rare:51; Clinvar:1 | ||||
chr3:49022026-49022141 | Rare:37 | ||||
chr3:49029365-49029668 | Common:2; Rare:186 | ||||
chr3:49094019-49094162 | Rare:29 | ||||
chr3:49104717-49104910 | Rare:83; Clinvar:1; Clinvar (benign):4 |