Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:47979490-47979764 | Common:1; Rare:107 | ||||
chr7:50450329-50450447 | Rare:49 | ||||
chr7:55366271-55366340 | Rare:23 | ||||
chr7:55572341-55572570 | Common:1; Rare:93 | ||||
chr7:56051544-56051840 | Rare:125; Clinvar:4 | ||||
chr7:56106385-56106511 | Common:6; Rare:59 | ||||
chr7:64794277-64794462 | Common:4; Rare:51 | ||||
chr7:65982188-65982328 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):3 | ||||
chr7:66114799-66114944 | Common:1; Rare:63 | ||||
chr7:66682050-66682170 | Common:5; Rare:51 | ||||
chr7:66921127-66921225 | Rare:35 | ||||
chr7:66996574-66996872 | Common:2; Rare:62 | ||||
chr7:73683399-73683622 | Common:3; Rare:91 | ||||
chr7:73738786-73739123 | Common:2; Rare:106 | ||||
chr7:73769610-73769861 | Common:1; Rare:77 |