Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:12117075-12117571 | Common:16; Rare:94 | ||||
chr16:15708838-15708906 | Rare:33; Clinvar:1; Clinvar (benign):2 | ||||
chr16:15719218-15719403 | Common:1; Rare:66; Clinvar:6; Clinvar (benign):3 | ||||
chr16:15719687-15719810 | Common:1; Rare:34; Clinvar (benign):2 | ||||
chr16:15727038-15727067 | Rare:10; Clinvar (benign):2 | ||||
chr16:21300815-21300936 | Common:2; Rare:22 | ||||
chr16:21520403-21520578 | Common:1; Rare:15 | ||||
chr16:21820398-21820484 | Rare:22 | ||||
chr16:22195794-22195903 | Common:4; Rare:57 | ||||
chr16:25107086-25107175 | Rare:24 | ||||
chr16:27332078-27332393 | Common:3; Rare:48 | ||||
chr16:29594688-29594864 | Common:5; Rare:54 | ||||
chr16:29595039-29595116 | Common:5; Rare:49 | ||||
chr16:30335356-30335606 | Common:2; Rare:83 | ||||
chr16:30634283-30634553 | Common:1; Rare:70 |