Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:6651553-6651767 | Common:1; Rare:76 | ||||
chr17:6995935-6996050 | Rare:23 | ||||
chr17:7012323-7012681 | Rare:123 | ||||
chr17:7241778-7241915 | Common:1; Rare:29 | ||||
chr17:7251963-7252313 | Common:1; Rare:137 | ||||
chr17:7307372-7307703 | Common:5; Rare:100 | ||||
chr17:7315069-7315560 | Common:4; Rare:178 | ||||
chr17:7438146-7438329 | Common:1; Rare:40 | ||||
chr17:7479517-7479730 | Common:1; Rare:37 | ||||
chr17:7484219-7484387 | Common:1; Rare:73 | ||||
chr17:7484697-7484834 | Rare:57 | ||||
chr17:7561758-7561999 | Common:2; Rare:70 | ||||
chr17:7583530-7583858 | Common:1; Rare:133; Clinvar:3; Clinvar (benign):3 | ||||
chr17:7843643-7843733 | Rare:32 | ||||
chr17:7857383-7857704 | Common:3; Rare:105 |