Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:94656122-94656372 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
chr7:95396346-95396573 | Common:2; Rare:91 | ||||
chr7:95596162-95596606 | Common:5; Rare:123 | ||||
chr7:96322016-96322171 | Rare:77; Clinvar:4 | ||||
chr7:98107103-98107234 | Common:1; Rare:37 | ||||
chr7:98252208-98252375 | Rare:39 | ||||
chr7:99325794-99325972 | Common:1; Rare:73 | ||||
chr7:99408537-99408665 | Common:2; Rare:43 | ||||
chr7:99408818-99409031 | Common:1; Rare:67 | ||||
chr7:99438744-99438985 | Common:1; Rare:70 | ||||
chr7:99500217-99500402 | Common:2; Rare:50 | ||||
chr7:99504513-99504680 | Rare:44 | ||||
chr7:99552075-99552164 | Rare:33 | ||||
chr7:99558497-99558894 | Common:4; Rare:119 | ||||
chr7:99919096-99919184 | Rare:30 |