Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44221200-44221427 | Rare:63 | ||||
chr17:44221555-44221790 | Common:4; Rare:69 | ||||
chr17:44222103-44222269 | Rare:33 | ||||
chr17:44268089-44268337 | Rare:50; Clinvar:3 | ||||
chr17:44324735-44325025 | Common:3; Rare:103 | ||||
chr17:44345082-44345334 | Rare:55; Clinvar:5; Clinvar (benign):4 | ||||
chr17:44352111-44352497 | Common:1; Rare:131; Clinvar:13; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr17:44385325-44385580 | Common:4; Rare:76; Clinvar:1 | ||||
chr17:44503371-44503714 | Rare:134 | ||||
chr17:44899368-44899774 | Common:3; Rare:127; Clinvar:3; Clinvar (benign):1 | ||||
chr17:44911499-44911596 | Common:3; Rare:27; Clinvar:2 | ||||
chr17:45051409-45051696 | Common:1; Rare:93 | ||||
chr17:45060987-45061393 | Common:2; Rare:122 | ||||
chr17:45132340-45132635 | Common:2; Rare:89 | ||||
chr17:45148120-45148631 | Common:1; Rare:171 |