Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37692183-37692592 | Common:5; Rare:98 | ||||
chr1:37807729-37807879 | Rare:55 | ||||
chr1:37807984-37808754 | Common:2; Rare:207 | ||||
chr1:37989953-37990114 | Rare:65 | ||||
chr1:38012524-38012826 | Rare:91 | ||||
chr1:38859676-38860031 | Rare:141 | ||||
chr1:38873291-38873563 | Common:3; Rare:93 | ||||
chr1:39026242-39026401 | Common:1; Rare:41 | ||||
chr1:39569595-39569933 | Common:1; Rare:101 | ||||
chr1:39954980-39955152 | Common:1; Rare:43 | ||||
chr1:40040455-40040799 | Common:3; Rare:103 | ||||
chr1:40161203-40161409 | Common:1; Rare:54 | ||||
chr1:40257741-40258390 | Common:5; Rare:171; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40508658-40508794 | Common:3; Rare:37 | ||||
chr1:40531470-40531591 | Rare:38 |