Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:27155155-27155359 | Common:3; Rare:69; Clinvar:5; Clinvar (benign):3 | ||||
chr10:27240516-27240650 | Common:2; Rare:41 | ||||
chr10:27242102-27242241 | Common:1; Rare:53 | ||||
chr10:28532622-28532784 | Common:1; Rare:68 | ||||
chr10:28532998-28533291 | Rare:121 | ||||
chr10:29634968-29635038 | Rare:14 | ||||
chr10:29647242-29647416 | Common:2; Rare:31 | ||||
chr10:29735754-29735853 | Common:1; Rare:18 | ||||
chr10:29736899-29737046 | Common:1; Rare:51 | ||||
chr10:30059487-30059678 | Common:1; Rare:71 | ||||
chr10:30433865-30434222 | Common:3; Rare:95 | ||||
chr10:31318991-31319285 | Common:2; Rare:80 | ||||
chr10:31928787-31928932 | Common:2; Rare:53 | ||||
chr10:32056375-32056557 | Common:1; Rare:74 | ||||
chr10:32446059-32446306 | Common:1; Rare:109 |