Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:39037564-39037701 | Common:1; Rare:49 | ||||
chr13:39037750-39037906 | Rare:52 | ||||
chr13:39037940-39038834 | Common:3; Rare:230 | ||||
chr13:39603098-39603367 | Common:2; Rare:94 | ||||
chr13:39603515-39603598 | Common:2; Rare:12 | ||||
chr13:39655532-39655915 | Common:7; Rare:174; Clinvar:3; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
chr13:40666536-40666805 | Common:2; Rare:96 | ||||
chr13:40770913-40770975 | Rare:23 | ||||
chr13:40771071-40771527 | Common:3; Rare:139 | ||||
chr13:40789264-40789644 | Common:3; Rare:129; Clinvar:6; Clinvar (benign):2 | ||||
chr13:40789667-40789855 | Common:1; Rare:51 | ||||
chr13:40982880-40983036 | Common:3; Rare:25 | ||||
chr13:41019254-41019450 | Rare:30 | ||||
chr13:41019731-41019796 | Rare:9 | ||||
chr13:41060054-41060581 | Common:3; Rare:187 |