Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11980120-11980483 | Common:6; Rare:122; Clinvar:1; Clinvar (benign):5 | ||||
chr1:12019263-12019575 | Common:5; Rare:110 | ||||
chr1:12617552-12617781 | Common:2; Rare:27 | ||||
chr1:13583543-13584391 | Common:5; Rare:308 | ||||
chr1:13584626-13584687 | Common:1; Rare:9 | ||||
chr1:13584722-13584880 | Common:2; Rare:31 | ||||
chr1:13699875-13700297 | Common:2; Rare:113 | ||||
chr1:13749264-13749483 | Common:1; Rare:83 | ||||
chr1:15152467-15152586 | Rare:19 | ||||
chr1:15153595-15153819 | Common:2; Rare:59 | ||||
chr1:15409813-15409984 | Rare:53 | ||||
chr1:15410210-15410260 | Rare:10 | ||||
chr1:15524197-15524577 | Common:2; Rare:95 | ||||
chr1:15526609-15526955 | Common:2; Rare:107 | ||||
chr1:15684243-15684391 | Common:1; Rare:47 |