Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:30594749-30594907 | Common:1; Rare:71; Clinvar:4; Clinvar (benign):3 | ||||
chr7:42932164-42932384 | Rare:82 | ||||
chr7:44573857-44574044 | Common:3; Rare:62 | ||||
chr7:56051550-56051788 | Rare:86; Clinvar:4 | ||||
chr7:66921140-66921456 | Common:1; Rare:95 | ||||
chr7:76047964-76048188 | Common:2; Rare:71 | ||||
chr7:77696253-77696467 | Rare:87 | ||||
chr7:91880685-91880739 | Rare:16 | ||||
chr7:92528480-92528811 | Common:3; Rare:100; Clinvar (benign):2 | ||||
chr7:94656109-94656371 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
chr7:99325805-99325963 | Common:1; Rare:61 | ||||
chr7:99408555-99408993 | Common:3; Rare:126 | ||||
chr7:99438768-99439027 | Common:2; Rare:68 | ||||
chr7:99466150-99466256 | Rare:33 | ||||
chr7:100119346-100119707 | Rare:107 |