Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:176238305-176238426 | Common:2; Rare:13 | ||||
chr5:176388550-176388806 | Common:4; Rare:98 | ||||
chr5:177022642-177022741 | Rare:37 | ||||
chr5:177133448-177133844 | Rare:141 | ||||
chr5:177303678-177304051 | Common:3; Rare:143 | ||||
chr5:177516932-177517063 | Rare:48; Clinvar (pathogenic):1 | ||||
chr5:177592073-177592290 | Common:2; Rare:98 | ||||
chr5:177592376-177592673 | Common:1; Rare:87 | ||||
chr5:178130872-178131045 | Rare:46 | ||||
chr5:178627005-178627231 | Common:6; Rare:79 | ||||
chr5:178940955-178941239 | Common:1; Rare:75 | ||||
chr5:179550524-179550561 | Common:2; Rare:7 | ||||
chr5:179559534-179559781 | Common:1; Rare:67 | ||||
chr5:179698591-179698612 | Rare:7 | ||||
chr5:179698620-179699092 | Common:4; Rare:162 |