Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:72727598-72727950 | Common:4; Rare:129 | ||||
chr13:72781896-72782180 | Common:1; Rare:107 | ||||
chr13:75549377-75549821 | Common:9; Rare:117 | ||||
chr13:94596144-94596369 | Common:2; Rare:71 | ||||
chr13:95676930-95677186 | Common:3; Rare:88 | ||||
chr13:96053374-96053557 | Common:2; Rare:76 | ||||
chr13:99200668-99200894 | Common:6; Rare:104 | ||||
chr13:100088941-100089117 | Rare:65; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596831-102597010 | Common:1; Rare:80 | ||||
chr13:102845734-102846097 | Common:8; Rare:95; Clinvar:2; Clinvar (benign):4 | ||||
chr13:106568097-106568261 | Rare:51 | ||||
chr13:108218358-108218532 | Rare:68 | ||||
chr14:20343240-20343635 | Common:11; Rare:227 | ||||
chr14:20684473-20684594 | Common:1; Rare:19; Clinvar (benign):1 | ||||
chr14:21476950-21477253 | Rare:84 |