Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:61304567-61304844 | Common:1; Rare:55 | ||||
chr5:61337560-61338113 | Rare:115 | ||||
chr5:61374892-61375097 | Rare:44 | ||||
chr5:61375271-61375502 | Rare:44 | ||||
chr5:61379054-61379348 | Rare:54 | ||||
chr5:61391895-61391898 | Rare:1 | ||||
chr5:61407901-61407916 | Rare:3 | ||||
chr5:61526178-61526556 | Rare:78; Clinvar (benign):1 | ||||
chr5:61538941-61539014 | Rare:9 | ||||
chr5:62392973-62393181 | Common:2; Rare:37 | ||||
chr5:64750478-64750573 | Rare:17 | ||||
chr5:65680544-65680655 | Rare:36 | ||||
chr5:65746230-65746322 | Rare:16 | ||||
chr5:65975497-65975625 | Rare:26 | ||||
chr5:66003274-66003305 | Rare:3 |