Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20484638-20484803 | Common:2; Rare:34 | ||||
chr1:20485604-20485984 | Common:1; Rare:65 | ||||
chr1:20486179-20486543 | Rare:86 | ||||
chr1:20486633-20486876 | Common:1; Rare:62 | ||||
chr1:20507526-20507867 | Common:1; Rare:58 | ||||
chr1:20508034-20508298 | Common:5; Rare:83 | ||||
chr1:20552098-20552144 | Rare:10 | ||||
chr1:20552327-20552594 | Rare:62 | ||||
chr1:20633317-20633523 | Rare:60 | ||||
chr1:20633817-20634046 | Common:1; Rare:92; Clinvar (benign):1 | ||||
chr1:20661307-20661928 | Common:4; Rare:205; Clinvar:4; Clinvar (benign):7 | ||||
chr1:20717703-20717725 | Rare:7 | ||||
chr1:20732124-20732444 | Common:1; Rare:67 | ||||
chr1:20733205-20733391 | Common:5; Rare:36 | ||||
chr1:20785936-20786044 | Rare:20 |