Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45500040-45500385 | Common:1; Rare:95; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521688-45522109 | Common:1; Rare:151 | ||||
chr1:45550699-45551115 | Common:3; Rare:106 | ||||
chr1:45583925-45584205 | Common:1; Rare:109 | ||||
chr1:45686479-45686691 | Rare:79 | ||||
chr1:45687054-45687357 | Common:1; Rare:80 | ||||
chr1:45688072-45688258 | Common:1; Rare:55 | ||||
chr1:45750607-45750808 | Rare:74 | ||||
chr1:46132614-46133244 | Common:3; Rare:189 | ||||
chr1:46133340-46133511 | Common:1; Rare:43 | ||||
chr1:46198358-46198534 | Common:1; Rare:73; Clinvar:1 | ||||
chr1:46247417-46247819 | Common:5; Rare:70 | ||||
chr1:46303162-46303820 | Common:3; Rare:200 | ||||
chr1:46340657-46340838 | Common:3; Rare:50 | ||||
chr1:46604196-46604449 | Common:1; Rare:67 |