Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154221239-154221383 | Rare:33 | ||||
chr1:154221426-154221570 | Rare:37 | ||||
chr1:154242339-154242538 | Common:1; Rare:27 | ||||
chr1:154272489-154272718 | Common:4; Rare:54; Clinvar:1; Clinvar (benign):3 | ||||
chr1:154405028-154405440 | Common:4; Rare:69 | ||||
chr1:154551787-154551964 | Rare:41 | ||||
chr1:154558614-154558951 | Common:1; Rare:78 | ||||
chr1:154627860-154628039 | Common:3; Rare:89 | ||||
chr1:154961359-154961529 | Rare:54 | ||||
chr1:154961695-154961831 | Rare:58 | ||||
chr1:154970082-154970482 | Common:1; Rare:128 | ||||
chr1:154970602-154970936 | Common:1; Rare:62 | ||||
chr1:154974288-154974698 | Rare:94 | ||||
chr1:155002050-155002939 | Common:4; Rare:177 | ||||
chr1:155051150-155051406 | Common:2; Rare:85 |