Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:204410882-204411491 | Common:2; Rare:250; Clinvar:1 | ||||
chr1:204411516-204412307 | Common:14; Rare:215 | ||||
chr1:204494356-204494416 | Rare:8 | ||||
chr1:204494630-204494937 | Common:1; Rare:100 | ||||
chr1:204516004-204516109 | Rare:19 | ||||
chr1:204516121-204516842 | Common:2; Rare:179 | ||||
chr1:204524975-204525131 | Rare:27 | ||||
chr1:205121733-205121784 | Common:1; Rare:10 | ||||
chr1:205121862-205122629 | Common:7; Rare:206 | ||||
chr1:205210935-205211847 | Common:2; Rare:277; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:205227765-205228001 | Common:1; Rare:76 | ||||
chr1:205228319-205228565 | Common:1; Rare:61 | ||||
chr1:205321685-205321924 | Common:3; Rare:75 | ||||
chr1:205449306-205449606 | Common:3; Rare:50 | ||||
chr1:205449884-205450235 | Common:3; Rare:108 |