Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:177022586-177022930 | Common:1; Rare:116 | ||||
chr5:177133427-177133870 | Rare:158 | ||||
chr5:177134174-177134431 | Rare:61 | ||||
chr5:177303655-177303868 | Common:4; Rare:105 | ||||
chr5:177351847-177352038 | Rare:47 | ||||
chr5:177425976-177426051 | Rare:17 | ||||
chr5:177426234-177426546 | Common:2; Rare:98 | ||||
chr5:177467253-177467646 | Common:1; Rare:118 | ||||
chr5:177472842-177472956 | Rare:31 | ||||
chr5:177473442-177473778 | Common:1; Rare:115 | ||||
chr5:177497548-177497755 | Common:1; Rare:77 | ||||
chr5:177516881-177517100 | Common:2; Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr5:177592015-177592252 | Common:1; Rare:88 | ||||
chr5:177600029-177600179 | Common:3; Rare:48; Clinvar (benign):1 | ||||
chr5:178113371-178113676 | Common:3; Rare:98 |