Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53946270-53946422 | Rare:62 | ||||
chr1:54053115-54053681 | Common:6; Rare:192 | ||||
chr1:54199993-54200202 | Rare:42 | ||||
chr1:54801279-54801371 | Rare:19 | ||||
chr1:54887168-54887367 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
chr1:58783964-58784391 | Common:1; Rare:116 | ||||
chr1:59296520-59296842 | Common:12; Rare:86 | ||||
chr1:61725090-61725417 | Common:2; Rare:124 | ||||
chr1:61742369-61742553 | Rare:54 | ||||
chr1:62436256-62436364 | Common:2; Rare:36 | ||||
chr1:62436769-62437031 | Rare:60 | ||||
chr1:62688271-62688510 | Common:1; Rare:96 | ||||
chr1:62784069-62784180 | Rare:44 | ||||
chr1:63523190-63523589 | Common:3; Rare:101 | ||||
chr1:63593041-63593321 | Rare:62 |