Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:177133486-177133804 | Rare:115 | ||||
chr5:177303683-177303880 | Common:3; Rare:93 | ||||
chr5:177516917-177516990 | Rare:38; Clinvar (pathogenic):1 | ||||
chr5:179559559-179559805 | Common:1; Rare:72 | ||||
chr5:179698610-179699099 | Common:4; Rare:174 | ||||
chr5:179858792-179859031 | Rare:126 | ||||
chr5:180802756-180802953 | Common:6; Rare:82 | ||||
chr5:181223122-181223313 | Rare:65 | ||||
chr5:181223633-181223743 | Common:2; Rare:25 | ||||
chr5:181243690-181243950 | Common:4; Rare:95 | ||||
chr5:181261086-181261220 | Rare:39 | ||||
chr6:2245427-2245834 | Common:1; Rare:136 | ||||
chr6:2971251-2971576 | Common:5; Rare:76 | ||||
chr6:2971580-2971867 | Common:1; Rare:74 | ||||
chr6:2999653-2999999 | Common:10; Rare:70 |