Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:39584032-39584388 | Common:1; Rare:101 | ||||
chr15:39585635-39586044 | Common:3; Rare:52 | ||||
chr15:43176690-43176948 | Common:2; Rare:43 | ||||
chr15:45200482-45200595 | Common:1; Rare:35 | ||||
chr15:48415705-48415998 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr15:51094651-51094976 | Common:8; Rare:86 | ||||
chr15:58821490-58821790 | Common:2; Rare:56 | ||||
chr15:58932367-58932655 | Common:1; Rare:57 | ||||
chr15:62657686-62657825 | Rare:33 | ||||
chr15:64963607-64963929 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):2 | ||||
chr15:67066707-67066946 | Common:1; Rare:45 | ||||
chr15:68369183-68369515 | Rare:81 | ||||
chr15:71165126-71165445 | Common:1; Rare:45 | ||||
chr15:72202601-72202652 | Rare:14 | ||||
chr15:73927786-73927879 | Rare:21 |