Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:176448136-176448405 | Common:1; Rare:93 | ||||
chr5:177022642-177022741 | Rare:37 | ||||
chr5:177303700-177303933 | Common:3; Rare:101 | ||||
chr5:177516932-177517079 | Rare:51; Clinvar (pathogenic):1 | ||||
chr5:178204362-178204534 | Common:3; Rare:59 | ||||
chr5:178940936-178941233 | Common:1; Rare:78 | ||||
chr5:179559546-179559814 | Common:1; Rare:76 | ||||
chr5:179623609-179623980 | Common:4; Rare:133 | ||||
chr5:179698685-179699099 | Common:3; Rare:136 | ||||
chr5:179806884-179807052 | Common:3; Rare:63 | ||||
chr5:179858797-179858993 | Rare:108 | ||||
chr5:179907828-179908080 | Common:4; Rare:120 | ||||
chr5:180353321-180353491 | Common:4; Rare:70 | ||||
chr5:180809837-180809922 | Common:1; Rare:21 | ||||
chr5:180810115-180810209 | Common:1; Rare:21 |