Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:43407766-43407851 | Common:1; Rare:35 | ||||
chr10:43409119-43409436 | Common:3; Rare:108 | ||||
chr10:43436545-43436903 | Common:4; Rare:112 | ||||
chr10:43574481-43574705 | Common:1; Rare:78 | ||||
chr10:44959580-44959837 | Common:2; Rare:78 | ||||
chr10:45000814-45000971 | Common:1; Rare:61 | ||||
chr10:45727164-45727292 | Common:1; Rare:50 | ||||
chr10:45972352-45972729 | Common:6; Rare:121 | ||||
chr10:48424274-48424561 | Common:1; Rare:50 | ||||
chr10:48604968-48605211 | Common:1; Rare:58 | ||||
chr10:49941914-49942275 | Rare:96 | ||||
chr10:50067866-50067999 | Common:2; Rare:65 | ||||
chr10:50623842-50624091 | Common:1; Rare:89 | ||||
chr10:50624545-50624728 | Common:4; Rare:67 | ||||
chr10:51074373-51074652 | Common:1; Rare:65; Clinvar (benign):6 |