Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:135054731-135054925 | Common:5; Rare:65 | ||||
chr6:135497604-135497936 | Common:4; Rare:126; Clinvar:1; Clinvar (benign):2 | ||||
chr6:135851967-135852017 | Rare:10 | ||||
chr6:136289316-136289483 | Rare:81 | ||||
chr6:136289747-136290063 | Common:2; Rare:141 | ||||
chr6:136526062-136526221 | Rare:26 | ||||
chr6:136526395-136526545 | Common:3; Rare:33 | ||||
chr6:136526629-136526667 | Rare:10 | ||||
chr6:137219113-137219502 | Common:5; Rare:140; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr6:138161849-138162076 | Common:5; Rare:77 | ||||
chr6:138572518-138572723 | Common:1; Rare:45 | ||||
chr6:138773701-138773863 | Common:3; Rare:76 | ||||
chr6:138988215-138988422 | Common:3; Rare:57 | ||||
chr6:139028469-139028538 | Rare:13 | ||||
chr6:139028553-139028906 | Common:1; Rare:71 |