Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207088232-207088548 | Common:1; Rare:50 | ||||
chr1:207088759-207088939 | Rare:24 | ||||
chr1:207089342-207089647 | Common:3; Rare:81 | ||||
chr1:207321044-207321375 | Common:3; Rare:77 | ||||
chr1:207321422-207321823 | Common:1; Rare:103 | ||||
chr1:207454166-207454364 | Common:2; Rare:43; Clinvar:1 | ||||
chr1:207751762-207752173 | Common:2; Rare:119 | ||||
chr1:207752283-207752443 | Rare:39 | ||||
chr1:207752481-207752544 | Rare:7 | ||||
chr1:208244278-208244540 | Common:1; Rare:78 | ||||
chr1:209651409-209651441 | Rare:5 | ||||
chr1:209652343-209652647 | Common:3; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
chr1:209675136-209675488 | Common:2; Rare:86 | ||||
chr1:209675581-209675657 | Common:1; Rare:19 | ||||
chr1:209780286-209780557 | Common:2; Rare:70 |