Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:169701989-169702383 | Common:5; Rare:163 | ||||
chr6:169751585-169751658 | Rare:33; Clinvar (benign):2 | ||||
chr6:170554180-170554404 | Common:1; Rare:69 | ||||
chr7:727225-727314 | Rare:32; Clinvar:1 | ||||
chr7:975507-975650 | Common:1; Rare:64 | ||||
chr7:2242176-2242270 | Common:2; Rare:54 | ||||
chr7:2354541-2354933 | Common:5; Rare:164 | ||||
chr7:2403304-2403637 | Common:1; Rare:130 | ||||
chr7:4775463-4775689 | Common:6; Rare:109; Clinvar:1 | ||||
chr7:5527980-5528412 | Common:1; Rare:137; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr7:5593429-5593663 | Common:1; Rare:71 | ||||
chr7:6009030-6009350 | Common:4; Rare:135; Clinvar:3; Clinvar (benign):14 | ||||
chr7:6272631-6272743 | Rare:38 | ||||
chr7:6484061-6484232 | Common:1; Rare:95 | ||||
chr7:19117627-19118015 | Common:1; Rare:87 |