Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:74254366-74254520 | Rare:70 | ||||
chr7:76047964-76048157 | Common:1; Rare:59 | ||||
chr7:76302890-76303003 | Rare:46; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr7:77696242-77696460 | Rare:85 | ||||
chr7:79453687-79454024 | Common:3; Rare:81 | ||||
chr7:80919035-80919348 | Common:3; Rare:112 | ||||
chr7:87152314-87152468 | Common:1; Rare:49 | ||||
chr7:87876294-87876643 | Common:2; Rare:156 | ||||
chr7:90346515-90346728 | Common:3; Rare:83 | ||||
chr7:92134442-92134604 | Rare:50 | ||||
chr7:92528431-92528807 | Common:3; Rare:118; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr7:93232189-93232379 | Common:2; Rare:37 | ||||
chr7:94656080-94656372 | Common:2; Rare:76; Clinvar:3; Clinvar (benign):3 | ||||
chr7:97117489-97117711 | Rare:79 | ||||
chr7:99325808-99325955 | Common:1; Rare:57 |