Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53945559-53946045 | Common:7; Rare:121 | ||||
chr1:53946254-53946701 | Common:3; Rare:137 | ||||
chr1:54052999-54053698 | Common:7; Rare:237 | ||||
chr1:54199988-54200255 | Rare:77 | ||||
chr1:54886702-54886845 | Rare:47 | ||||
chr1:54886892-54887075 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
chr1:55215346-55215414 | Rare:33 | ||||
chr1:56645295-56645375 | Common:1; Rare:29 | ||||
chr1:58699994-58700191 | Common:4; Rare:90 | ||||
chr1:58783965-58784083 | Rare:37 | ||||
chr1:59296530-59296884 | Common:12; Rare:94 | ||||
chr1:62552877-62552998 | Rare:33; Clinvar:2 | ||||
chr1:62688236-62688544 | Common:1; Rare:113; Clinvar:1 | ||||
chr1:63523155-63523579 | Common:3; Rare:118 | ||||
chr1:63593194-63593514 | Rare:120; Clinvar (benign):2 |