Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151326946-151327133 | Rare:35 | ||||
chr1:151327293-151327446 | Common:1; Rare:44 | ||||
chr1:151327663-151327871 | Common:3; Rare:46 | ||||
chr1:151346278-151346342 | Rare:15; Clinvar:1 | ||||
chr1:151346957-151347295 | Rare:68 | ||||
chr1:151347615-151347790 | Common:2; Rare:24 | ||||
chr1:151399378-151399634 | Common:3; Rare:82; Clinvar (pathogenic):2 | ||||
chr1:151458527-151458900 | Common:5; Rare:203 | ||||
chr1:151459074-151459248 | Common:1; Rare:55 | ||||
chr1:151459412-151459571 | Rare:68 | ||||
chr1:151511155-151511397 | Common:3; Rare:55 | ||||
chr1:151540137-151540316 | Rare:50 | ||||
chr1:151763432-151763714 | Common:3; Rare:104 | ||||
chr1:151790456-151790874 | Common:3; Rare:98 | ||||
chr1:151909339-151909805 | Common:4; Rare:163 |