Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:172770968-172771218 | Common:2; Rare:78 | ||||
chr5:172771240-172771470 | Common:2; Rare:93 | ||||
chr5:172904978-172905233 | Common:1; Rare:45 | ||||
chr5:172959370-172959467 | Common:1; Rare:38 | ||||
chr5:173890505-173890659 | Rare:46 | ||||
chr5:176361762-176361896 | Common:1; Rare:37 | ||||
chr5:176388561-176388816 | Common:4; Rare:101 | ||||
chr5:176448162-176448413 | Common:1; Rare:86 | ||||
chr5:177022635-177022737 | Rare:35 | ||||
chr5:177133402-177133633 | Rare:71 | ||||
chr5:177303678-177303998 | Common:3; Rare:130 | ||||
chr5:177516921-177517093 | Rare:61; Clinvar (pathogenic):1 | ||||
chr5:178130848-178131039 | Rare:52 | ||||
chr5:178153735-178153957 | Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
chr5:179559546-179559765 | Common:1; Rare:60 |