Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243101667-243101909 | Common:11; Rare:148 | ||||
chr1:243455802-243456055 | Common:2; Rare:49 | ||||
chr1:243456270-243456444 | Rare:31 | ||||
chr1:243739623-243739916 | Rare:57 | ||||
chr1:244451138-244451248 | Common:2; Rare:29 | ||||
chr1:244863734-244863852 | Rare:39; Clinvar:1; Clinvar (benign):2 | ||||
chr1:245051485-245051673 | Common:2; Rare:25 | ||||
chr1:247855278-247855443 | Common:1; Rare:29 | ||||
chr10:3435703-3435859 | Rare:34 | ||||
chr10:4880162-4880226 | Common:1; Rare:9 | ||||
chr10:4916216-4916412 | Rare:33 | ||||
chr10:5099171-5099444 | Common:4; Rare:95 | ||||
chr10:5183682-5183970 | Common:3; Rare:54 | ||||
chr10:6163640-6163869 | Common:6; Rare:78 | ||||
chr10:13765843-13766013 | Rare:33 |