Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:179820713-179820930 | Common:6; Rare:85; Clinvar:1; Clinvar (benign):2 | ||||
chr5:179858797-179858993 | Rare:108 | ||||
chr5:180649571-180649709 | Rare:48 | ||||
chr5:180802760-180802976 | Common:8; Rare:85 | ||||
chr5:180810108-180810230 | Common:1; Rare:28 | ||||
chr5:180861146-180861394 | Common:2; Rare:99 | ||||
chr5:181223118-181223313 | Rare:66 | ||||
chr5:181223559-181223761 | Common:3; Rare:45 | ||||
chr5:181243690-181243776 | Rare:21 | ||||
chr5:181261060-181261286 | Rare:78 | ||||
chr6:292450-292542 | Rare:31 | ||||
chr6:693039-693209 | Rare:56 | ||||
chr6:2245425-2245825 | Common:1; Rare:134 | ||||
chr6:2902815-2902888 | Rare:12 | ||||
chr6:2971259-2971473 | Common:4; Rare:53 |