Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:140718809-140718925 | Common:3; Rare:42 | ||||
chr5:143041673-143041889 | Common:3; Rare:41; Clinvar (pathogenic):1 | ||||
chr5:149932876-149933044 | Rare:26 | ||||
chr5:149958095-149958305 | Common:4; Rare:41 | ||||
chr5:150778671-150778833 | Rare:66 | ||||
chr5:160165240-160165432 | Rare:34 | ||||
chr5:160165775-160165993 | Common:1; Rare:42 | ||||
chr5:173455377-173455402 | Rare:2 | ||||
chr5:173472318-173472545 | Common:2; Rare:38 | ||||
chr5:175382256-175382371 | Common:2; Rare:17 | ||||
chr5:177096078-177096348 | Common:1; Rare:80 | ||||
chr5:177098588-177098690 | Rare:22 | ||||
chr5:178115256-178115471 | Common:1; Rare:58 | ||||
chr5:178116104-178116160 | Rare:7 | ||||
chr5:178118569-178118807 | Rare:53 |