Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:66115179-66115353 | Rare:40 | ||||
chr7:66682028-66682172 | Common:5; Rare:69 | ||||
chr7:66996557-66996850 | Common:2; Rare:65 | ||||
chr7:73683419-73683622 | Common:3; Rare:81 | ||||
chr7:73738798-73739017 | Common:1; Rare:64 | ||||
chr7:74174031-74174396 | Common:1; Rare:166 | ||||
chr7:74254366-74254520 | Rare:70 | ||||
chr7:75914944-75915164 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
chr7:75994511-75994741 | Common:3; Rare:113 | ||||
chr7:76047950-76048201 | Common:2; Rare:86 | ||||
chr7:76302877-76303075 | Rare:83; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr7:76303456-76303865 | Common:2; Rare:174; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
chr7:77199701-77199990 | Common:2; Rare:66 | ||||
chr7:77696231-77696481 | Rare:102 | ||||
chr7:77798455-77798971 | Common:1; Rare:129 |