Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:35801801-35801830 | Rare:10 | ||||
chr7:44884684-44884789 | Rare:47 | ||||
chr7:44986585-44986790 | Common:2; Rare:99 | ||||
chr7:45768920-45769158 | Common:2; Rare:77 | ||||
chr7:65750918-65751080 | Common:2; Rare:64 | ||||
chr7:66493512-66493762 | Common:4; Rare:107 | ||||
chr7:66592334-66592482 | Common:2; Rare:52 | ||||
chr7:66654391-66654594 | Common:1; Rare:81 | ||||
chr7:67302400-67302737 | Common:5; Rare:108 | ||||
chr7:73005867-73006140 | Rare:26 | ||||
chr7:74890556-74890833 | Common:2; Rare:86 | ||||
chr7:75359020-75359253 | Rare:6 | ||||
chr7:94392139-94392236 | Common:2; Rare:12 | ||||
chr7:94409318-94409608 | Rare:83; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr7:94410001-94410526 | Common:2; Rare:107; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 |