Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53946540-53946564 | Rare:7 | ||||
chr1:54052679-54052832 | Common:1; Rare:31 | ||||
chr1:54053155-54053338 | Rare:61 | ||||
chr1:54053360-54053759 | Common:6; Rare:125 | ||||
chr1:54054023-54054069 | Common:1; Rare:8 | ||||
chr1:54199963-54200273 | Rare:89 | ||||
chr1:54406327-54406604 | Common:4; Rare:120 | ||||
chr1:54542077-54542236 | Common:2; Rare:52 | ||||
chr1:54542252-54542558 | Common:2; Rare:79 | ||||
chr1:54715710-54716043 | Common:4; Rare:101 | ||||
chr1:54716045-54716149 | Rare:34 | ||||
chr1:54763780-54764055 | Common:1; Rare:53 | ||||
chr1:54764399-54764864 | Common:7; Rare:138; Clinvar (benign):1 | ||||
chr1:54886440-54886887 | Common:1; Rare:152 | ||||
chr1:54886968-54887021 | Rare:19; Clinvar:1 |