Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:38176650-38176897 | Common:5; Rare:69 | ||||
chr8:38269125-38269264 | Rare:55 | ||||
chr8:38381901-38382080 | Common:1; Rare:42 | ||||
chr8:38996226-38996299 | Common:1; Rare:36 | ||||
chr8:38996443-38997072 | Common:7; Rare:239 | ||||
chr8:40153332-40153568 | Common:2; Rare:64 | ||||
chr8:41577975-41578249 | Rare:86 | ||||
chr8:42271243-42271469 | Common:2; Rare:86 | ||||
chr8:42391743-42391925 | Common:2; Rare:64 | ||||
chr8:42541116-42541179 | Rare:13 | ||||
chr8:42541494-42541661 | Common:2; Rare:45 | ||||
chr8:42541678-42542010 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
chr8:42843213-42843499 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):3 | ||||
chr8:42896590-42897043 | Common:1; Rare:183 | ||||
chr8:43056132-43056463 | Common:1; Rare:120 |