Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7308844-7308971 | Rare:30 | ||||
chr17:7313412-7313621 | Common:1; Rare:90 | ||||
chr17:7315004-7315437 | Common:4; Rare:154 | ||||
chr17:7350176-7350421 | Common:2; Rare:75 | ||||
chr17:7351619-7351738 | Rare:22 | ||||
chr17:7352041-7352212 | Rare:58 | ||||
chr17:7405092-7405157 | Rare:11 | ||||
chr17:7479479-7479713 | Common:1; Rare:40 | ||||
chr17:7484194-7484391 | Common:2; Rare:86 | ||||
chr17:7484690-7484852 | Rare:64 | ||||
chr17:7499161-7499318 | Common:2; Rare:48 | ||||
chr17:7549033-7549281 | Common:3; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr17:7558214-7558325 | Rare:28 | ||||
chr17:7558371-7558706 | Rare:69 | ||||
chr17:7558710-7559035 | Common:1; Rare:65 |