Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1783914-1784052 | Common:1; Rare:27 | ||||
chr17:1829689-1830082 | Common:8; Rare:152 | ||||
chr17:2029987-2030219 | Common:1; Rare:96; Clinvar (pathogenic):1 | ||||
chr17:2030657-2030825 | Rare:33 | ||||
chr17:2041848-2042196 | Common:6; Rare:170 | ||||
chr17:2053907-2054172 | Common:3; Rare:92 | ||||
chr17:2054950-2055154 | Rare:56 | ||||
chr17:2055894-2056097 | Rare:50 | ||||
chr17:2056728-2056903 | Rare:41 | ||||
chr17:2082257-2082494 | Common:1; Rare:37 | ||||
chr17:2088644-2088714 | Common:1; Rare:12 | ||||
chr17:2239876-2240157 | Rare:58 | ||||
chr17:2240165-2240553 | Common:1; Rare:73 | ||||
chr17:2266168-2266368 | Common:2; Rare:36 | ||||
chr17:2266645-2266831 | Common:1; Rare:49 |