Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54887147-54887475 | Common:3; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
chr1:55039357-55039647 | Common:2; Rare:66; Clinvar:4; Clinvar (benign):1 | ||||
chr1:55214597-55214974 | Common:3; Rare:112 | ||||
chr1:55215099-55215171 | Rare:21 | ||||
chr1:55215286-55215689 | Common:2; Rare:142 | ||||
chr1:56579222-56579506 | Common:3; Rare:64 | ||||
chr1:56579527-56579577 | Rare:13 | ||||
chr1:56645199-56645394 | Common:1; Rare:70 | ||||
chr1:57423941-57424430 | Common:5; Rare:130 | ||||
chr1:57424511-57424612 | Common:1; Rare:17 | ||||
chr1:58546182-58546429 | Common:4; Rare:56 | ||||
chr1:58546553-58546967 | Common:4; Rare:127 | ||||
chr1:58699965-58700209 | Common:4; Rare:110 | ||||
chr1:58783835-58784488 | Common:2; Rare:177 | ||||
chr1:58784563-58784803 | Common:3; Rare:64 |