Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99659247-99659547 | Common:1; Rare:77 | ||||
chr10:99732056-99732329 | Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185938-100186187 | Rare:97 | ||||
chr10:100229553-100229690 | Rare:50 | ||||
chr10:100286631-100286759 | Common:3; Rare:68 | ||||
chr10:100347444-100347482 | Rare:12 | ||||
chr10:100529836-100530006 | Common:1; Rare:45 | ||||
chr10:100535906-100535961 | Rare:21 | ||||
chr10:100912751-100913056 | Common:1; Rare:91 | ||||
chr10:100913335-100913468 | Rare:32 | ||||
chr10:100987090-100987584 | Common:1; Rare:179; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031117-101031285 | Common:1; Rare:36 | ||||
chr10:101588202-101588339 | Rare:55 | ||||
chr10:101694831-101695250 | Common:1; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
chr10:101818349-101818762 | Common:1; Rare:111 |