Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:174283612-174283965 | Common:1; Rare:71 | ||||
chr4:176319850-176320085 | Common:3; Rare:92 | ||||
chr4:177442376-177442554 | Rare:105; Clinvar:2 | ||||
chr4:183444547-183444701 | Rare:74 | ||||
chr4:183659049-183659404 | Common:1; Rare:110 | ||||
chr4:184474508-184474829 | Rare:74 | ||||
chr4:184649399-184649826 | Common:4; Rare:139 | ||||
chr4:185425870-185426034 | Common:2; Rare:61 | ||||
chr4:186191544-186191814 | Common:4; Rare:89; Clinvar:1; Clinvar (benign):4 | ||||
chr4:189940620-189940964 | Common:9; Rare:122 | ||||
chr5:218093-218415 | Common:4; Rare:128; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr5:321571-321763 | Common:2; Rare:42 | ||||
chr5:443095-443287 | Common:9; Rare:89 | ||||
chr5:892520-893013 | Common:5; Rare:158 | ||||
chr5:1799778-1799993 | Common:8; Rare:101 |