Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:47478067-47478232 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
chr6:49463180-49463431 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
chr6:52284676-52284920 | Common:2; Rare:96 | ||||
chr6:52420108-52420364 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
chr6:52995267-52995807 | Common:4; Rare:227 | ||||
chr6:53061727-53062053 | Rare:72 | ||||
chr6:53065340-53065598 | Common:1; Rare:84 | ||||
chr6:53348892-53349204 | Common:2; Rare:118 | ||||
chr6:57172574-57172810 | Common:1; Rare:73 | ||||
chr6:57317547-57317674 | Rare:40 | ||||
chr6:63572265-63572560 | Rare:112 | ||||
chr6:69796877-69797187 | Common:1; Rare:89; Clinvar:6; Clinvar (benign):2 | ||||
chr6:70413188-70413437 | Common:1; Rare:69 | ||||
chr6:73521165-73521406 | Rare:45 | ||||
chr6:73521555-73521619 | Rare:17 |