Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:33285677-33285857 | Rare:35 | ||||
chr13:34942138-34942298 | Common:3; Rare:44 | ||||
chr13:36346301-36346454 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
chr13:37000768-37000821 | Rare:28; Clinvar (pathogenic):1 | ||||
chr13:37059621-37059741 | Common:1; Rare:38 | ||||
chr13:38349511-38349911 | Common:4; Rare:132; Clinvar (pathogenic):1 | ||||
chr13:38350208-38350363 | Rare:53 | ||||
chr13:39037818-39038056 | Common:1; Rare:76 | ||||
chr13:39038079-39038429 | Common:1; Rare:88 | ||||
chr13:40771145-40771346 | Common:3; Rare:63 | ||||
chr13:40789329-40789635 | Common:2; Rare:106; Clinvar:6; Clinvar (benign):2 | ||||
chr13:41060486-41060508 | Rare:6 | ||||
chr13:41060846-41061068 | Common:16; Rare:131 | ||||
chr13:41061151-41061590 | Common:4; Rare:146 | ||||
chr13:41132759-41132943 | Rare:44 |