Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:17580012-17580282 | Common:1; Rare:43 | ||||
chr1:18107006-18107349 | Common:1; Rare:53 | ||||
chr1:19210071-19210533 | Common:1; Rare:150 | ||||
chr1:19251506-19251848 | Common:6; Rare:112 | ||||
chr1:19311972-19312373 | Common:8; Rare:179 | ||||
chr1:19485435-19485751 | Common:1; Rare:112 | ||||
chr1:19596871-19597064 | Common:2; Rare:90 | ||||
chr1:19799676-19799987 | Common:5; Rare:96 | ||||
chr1:20486188-20486379 | Rare:45 | ||||
chr1:20508063-20508205 | Common:2; Rare:52 | ||||
chr1:20652952-20652992 | Rare:12; Clinvar (benign):2 | ||||
chr1:20660960-20661268 | Common:3; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
chr1:20661340-20661750 | Common:3; Rare:149; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786566-20786786 | Rare:78 | ||||
chr1:20786791-20786859 | Rare:27 |