Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:123023914-123024157 | Common:5; Rare:64 | ||||
chr5:124629291-124629494 | Common:4; Rare:36 | ||||
chr5:124743641-124743861 | Common:1; Rare:33 | ||||
chr5:124747356-124747681 | Rare:63 | ||||
chr5:124749353-124749563 | Rare:49 | ||||
chr5:128082956-128083159 | Common:2; Rare:59 | ||||
chr5:128287306-128287613 | Common:3; Rare:62; Clinvar:2; Clinvar (benign):4 | ||||
chr5:128395251-128395438 | Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
chr5:128513948-128514050 | Common:5; Rare:21 | ||||
chr5:128536258-128536481 | Common:1; Rare:65; Clinvar (benign):3 | ||||
chr5:129459576-129459718 | Rare:37 | ||||
chr5:134506215-134506520 | Common:1; Rare:61 | ||||
chr5:138464087-138464277 | Rare:62 | ||||
chr5:139698723-139698941 | Rare:34 | ||||
chr5:140868939-140868996 | Common:2; Rare:11 |