Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:159263236-159263321 | Common:1; Rare:26 | ||||
chr5:160419048-160419275 | Common:4; Rare:84 | ||||
chr5:163460331-163460665 | Common:5; Rare:74 | ||||
chr5:169583609-169583801 | Common:6; Rare:60 | ||||
chr5:171387531-171387993 | Rare:221; Clinvar:1 | ||||
chr5:172771183-172771470 | Common:4; Rare:115 | ||||
chr5:172834163-172834402 | Common:1; Rare:58 | ||||
chr5:172904992-172905233 | Common:1; Rare:41 | ||||
chr5:172958836-172958876 | Rare:9 | ||||
chr5:173328406-173328602 | Rare:37 | ||||
chr5:176388558-176388803 | Common:4; Rare:90 | ||||
chr5:177022647-177022741 | Rare:37 | ||||
chr5:177351643-177351968 | Rare:82 | ||||
chr5:177516932-177517083 | Rare:52; Clinvar (pathogenic):1 | ||||
chr5:177592051-177592223 | Common:1; Rare:62 |