Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:135510074-135510279 | Common:2; Rare:43 | ||||
chr7:135662357-135662551 | Common:4; Rare:87 | ||||
chr7:135977294-135977530 | Common:2; Rare:92 | ||||
chr7:137343466-137343641 | Rare:67 | ||||
chr7:139109337-139109492 | Common:1; Rare:46 | ||||
chr7:139341230-139341369 | Rare:29 | ||||
chr7:139359432-139359516 | Rare:31 | ||||
chr7:139359672-139359977 | Common:3; Rare:122 | ||||
chr7:141551342-141551434 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
chr7:141738021-141738468 | Common:4; Rare:134 | ||||
chr7:142854990-142855174 | Common:3; Rare:52 | ||||
chr7:143380886-143381388 | Common:2; Rare:155 | ||||
chr7:143382008-143382064 | Rare:15 | ||||
chr7:144836051-144836126 | Rare:26 | ||||
chr7:149028636-149028938 | Common:2; Rare:96 |