Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:30906579-30906738 | Common:2; Rare:46 | ||||
chr13:33285710-33285890 | Rare:42 | ||||
chr13:36346275-36346542 | Common:3; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
chr13:37000219-37000404 | Common:2; Rare:34 | ||||
chr13:37000774-37000805 | Rare:15 | ||||
chr13:37869730-37869922 | Common:1; Rare:46 | ||||
chr13:39037989-39038484 | Common:1; Rare:127 | ||||
chr13:40771145-40771440 | Common:3; Rare:84 | ||||
chr13:41060892-41061590 | Common:20; Rare:272 | ||||
chr13:41132705-41132974 | Rare:70 | ||||
chr13:41457405-41457555 | Common:2; Rare:47 | ||||
chr13:43879478-43879573 | Rare:27 | ||||
chr13:43879656-43879875 | Common:18; Rare:63 | ||||
chr13:44989449-44989607 | Rare:58 | ||||
chr13:45120388-45120513 | Common:1; Rare:39 |