Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41688730-41688888 | Common:1; Rare:54 | ||||
chr17:42017412-42017510 | Common:1; Rare:36 | ||||
chr17:42609348-42609711 | Common:7; Rare:148; Clinvar (benign):1 | ||||
chr17:47189284-47189587 | Rare:72 | ||||
chr17:48944741-48944864 | Common:1; Rare:47 | ||||
chr17:51260373-51260575 | Common:3; Rare:93 | ||||
chr17:54968631-54968779 | Common:3; Rare:71 | ||||
chr17:59106707-59106970 | Common:2; Rare:86; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59619596-59619962 | Common:3; Rare:132 | ||||
chr17:59707409-59707665 | Common:3; Rare:72; Clinvar (benign):1 | ||||
chr17:59892924-59893132 | Rare:61 | ||||
chr17:63773534-63773828 | Common:2; Rare:98 | ||||
chr17:68247873-68248115 | Common:5; Rare:104 | ||||
chr17:73232239-73232707 | Common:3; Rare:168 | ||||
chr17:74776335-74776540 | Common:4; Rare:66 |