Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:57501005-57501175 | Common:1; Rare:73 | ||||
chr11:57514798-57514950 | Rare:28 | ||||
chr11:57530696-57531067 | Common:1; Rare:88 | ||||
chr11:57567589-57567867 | Rare:85 | ||||
chr11:57606003-57606547 | Rare:146; Clinvar:1; Clinvar (benign):2 | ||||
chr11:57712166-57712743 | Common:10; Rare:199 | ||||
chr11:57741243-57741641 | Common:3; Rare:154 | ||||
chr11:58578090-58578138 | Rare:14 | ||||
chr11:58578340-58578530 | Common:2; Rare:72 | ||||
chr11:58578807-58579192 | Common:5; Rare:118 | ||||
chr11:58939362-58939648 | Common:3; Rare:50 | ||||
chr11:59142681-59142945 | Common:1; Rare:48 | ||||
chr11:60902581-60902746 | Rare:29 | ||||
chr11:60902855-60902912 | Rare:11 | ||||
chr11:60906369-60906832 | Common:1; Rare:122 |