Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:65081226-65081404 | Common:2; Rare:59 | ||||
chr7:65750282-65750477 | Common:3; Rare:40 | ||||
chr7:65750900-65751094 | Common:2; Rare:81 | ||||
chr7:65770719-65770923 | Common:6; Rare:64 | ||||
chr7:66493538-66493762 | Common:3; Rare:95 | ||||
chr7:66592315-66592437 | Common:2; Rare:43 | ||||
chr7:66654262-66654576 | Common:2; Rare:103 | ||||
chr7:66844872-66845061 | Common:2; Rare:77 | ||||
chr7:67302394-67302742 | Common:5; Rare:112 | ||||
chr7:72836602-72836863 | Common:1; Rare:44 | ||||
chr7:73005886-73006148 | Rare:22 | ||||
chr7:74060119-74060441 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr7:74890525-74890836 | Common:3; Rare:105 | ||||
chr7:75358976-75359239 | Common:1; Rare:7 | ||||
chr7:77196771-77197188 | Common:1; Rare:90 |