Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53196668-53196807 | Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
chr1:53220586-53220691 | Common:1; Rare:45 | ||||
chr1:53238424-53238598 | Rare:69 | ||||
chr1:53946253-53946482 | Rare:82 | ||||
chr1:54053000-54053152 | Common:1; Rare:56 | ||||
chr1:54053155-54053654 | Common:6; Rare:170 | ||||
chr1:54199988-54200226 | Rare:59 | ||||
chr1:54715689-54715894 | Common:4; Rare:61 | ||||
chr1:54801271-54801371 | Rare:20 | ||||
chr1:54886714-54886845 | Rare:43 | ||||
chr1:54886867-54887253 | Common:2; Rare:137; Clinvar:6; Clinvar (benign):2 | ||||
chr1:55039317-55039630 | Common:2; Rare:73; Clinvar:4; Clinvar (benign):1 | ||||
chr1:55215351-55215429 | Rare:39 | ||||
chr1:56645291-56645384 | Common:1; Rare:35 | ||||
chr1:58546672-58546850 | Common:4; Rare:79 |