Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:173144367-173144564 | Common:1; Rare:54 | ||||
chr5:173328383-173328583 | Rare:39 | ||||
chr5:176361738-176361886 | Rare:42 | ||||
chr5:176388550-176388811 | Common:4; Rare:103 | ||||
chr5:177022628-177022741 | Rare:43 | ||||
chr5:177133465-177133844 | Rare:139 | ||||
chr5:177303678-177304035 | Common:3; Rare:141 | ||||
chr5:177497575-177497832 | Common:1; Rare:95 | ||||
chr5:177516906-177517048 | Common:1; Rare:59; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr5:179559560-179559803 | Common:1; Rare:71 | ||||
chr5:179698603-179699102 | Common:4; Rare:178 | ||||
chr5:179806910-179807086 | Common:2; Rare:54 | ||||
chr5:179820713-179820939 | Common:6; Rare:91; Clinvar:1; Clinvar (benign):2 | ||||
chr5:179858796-179859007 | Rare:112 | ||||
chr5:180353313-180353524 | Common:5; Rare:94 |