Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:135170420-135170999 | Common:7; Rare:189 | ||||
chr7:135662383-135662559 | Common:3; Rare:87 | ||||
chr7:139231016-139231294 | Common:2; Rare:107 | ||||
chr7:139341234-139341380 | Rare:34 | ||||
chr7:139359692-139360087 | Common:3; Rare:146 | ||||
chr7:139483652-139483870 | Common:3; Rare:72 | ||||
chr7:140177044-140177329 | Common:2; Rare:107 | ||||
chr7:141551342-141551428 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
chr7:141738031-141738464 | Common:4; Rare:133 | ||||
chr7:142854990-142855138 | Common:2; Rare:44 | ||||
chr7:143263398-143263517 | Rare:35 | ||||
chr7:143288282-143288442 | Common:1; Rare:67 | ||||
chr7:143380954-143381293 | Common:1; Rare:107 | ||||
chr7:144835966-144836088 | Common:1; Rare:35; Clinvar (benign):2 | ||||
chr7:148698602-148698945 | Common:1; Rare:122 |