Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209220304-209220482 | Rare:30 | ||||
chr1:211382607-211382849 | Common:2; Rare:90 | ||||
chr1:218345272-218345353 | Rare:14 | ||||
chr1:218348124-218348299 | Common:1; Rare:45 | ||||
chr1:219927947-219927990 | Rare:14 | ||||
chr1:220253491-220253572 | Rare:19 | ||||
chr1:220527393-220527493 | Rare:20 | ||||
chr1:222814976-222815144 | Common:1; Rare:61 | ||||
chr1:223992564-223992834 | Common:4; Rare:94 | ||||
chr1:226703542-226703618 | Rare:27 | ||||
chr1:228275990-228276121 | Common:1; Rare:43 | ||||
chr1:228464603-228464881 | Common:1; Rare:68 | ||||
chr1:234611406-234611429 | Common:1; Rare:10 | ||||
chr1:243344003-243344309 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:243471967-243471989 | Rare:5 |