Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:172959288-172959460 | Common:2; Rare:57 | ||||
chr5:173328097-173328555 | Common:1; Rare:107 | ||||
chr5:176388986-176389208 | Rare:64 | ||||
chr5:177022600-177022741 | Common:1; Rare:58 | ||||
chr5:177303678-177303824 | Common:3; Rare:67 | ||||
chr5:177516903-177517079 | Common:1; Rare:69; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr5:178153809-178154116 | Rare:93; Clinvar:5; Clinvar (benign):1 | ||||
chr5:179698595-179699096 | Common:4; Rare:178 | ||||
chr5:179806307-179806432 | Rare:40 | ||||
chr5:179806864-179807063 | Common:3; Rare:79 | ||||
chr5:179823994-179824318 | Common:1; Rare:128; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr5:179858798-179858958 | Rare:91 | ||||
chr5:180810095-180810295 | Common:5; Rare:61 | ||||
chr5:181261124-181261262 | Rare:45 | ||||
chr6:693074-693198 | Rare:38 |