Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:177006557-177006893 | Common:4; Rare:104 | ||||
chr5:177022620-177022741 | Rare:45 | ||||
chr5:177133463-177133800 | Rare:121 | ||||
chr5:177133992-177134193 | Common:1; Rare:53 | ||||
chr5:177303685-177304075 | Common:3; Rare:146 | ||||
chr5:177351643-177351685 | Rare:11 | ||||
chr5:177483930-177484083 | Rare:50 | ||||
chr5:177496791-177497040 | Common:3; Rare:61 | ||||
chr5:177516881-177517098 | Common:2; Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr5:177600057-177600224 | Common:4; Rare:61; Clinvar (benign):5 | ||||
chr5:178153763-178154110 | Rare:107; Clinvar:5; Clinvar (benign):1 | ||||
chr5:178204337-178204534 | Common:3; Rare:69 | ||||
chr5:178232555-178232898 | Common:4; Rare:112 | ||||
chr5:178627015-178627231 | Common:6; Rare:76 | ||||
chr5:178941109-178941239 | Rare:34 |