Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:135148028-135148087 | Rare:14 | ||||
chr7:135170430-135170809 | Common:3; Rare:134 | ||||
chr7:135662406-135662544 | Common:2; Rare:63 | ||||
chr7:139109334-139109460 | Common:1; Rare:38 | ||||
chr7:139341234-139341380 | Rare:34 | ||||
chr7:139359692-139359968 | Common:2; Rare:113 | ||||
chr7:140696629-140696799 | Common:1; Rare:65 | ||||
chr7:140924211-140924237 | Rare:5 | ||||
chr7:141551265-141551423 | Common:1; Rare:47; Clinvar:5; Clinvar (benign):2 | ||||
chr7:141738021-141738468 | Common:4; Rare:134 | ||||
chr7:143882810-143882949 | Rare:33 | ||||
chr7:143902121-143902304 | Common:5; Rare:58 | ||||
chr7:144836026-144836156 | Common:1; Rare:46 | ||||
chr7:149028409-149028828 | Common:7; Rare:168 | ||||
chr7:149090672-149090908 | Rare:63 |