Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:27242031-27242243 | Common:1; Rare:94 | ||||
chr10:27504049-27504437 | Rare:171; Clinvar:5; Clinvar (benign):1 | ||||
chr10:28532702-28532896 | Common:1; Rare:69 | ||||
chr10:28532998-28533538 | Common:1; Rare:212 | ||||
chr10:28533566-28533616 | Rare:15 | ||||
chr10:29486083-29486497 | Rare:106 | ||||
chr10:29634899-29635053 | Rare:34 | ||||
chr10:29735768-29736000 | Common:3; Rare:44 | ||||
chr10:29736802-29737097 | Common:2; Rare:81 | ||||
chr10:30059491-30059689 | Common:1; Rare:73 | ||||
chr10:30433912-30434214 | Common:3; Rare:79 | ||||
chr10:30434605-30434711 | Common:1; Rare:31 | ||||
chr10:31031841-31032060 | Common:2; Rare:91 | ||||
chr10:31032326-31032611 | Common:13; Rare:91 | ||||
chr10:31318335-31318824 | Common:3; Rare:119 |