Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:89638721-89638824 | Common:3; Rare:36 | ||||
chr6:89829614-89829942 | Rare:82 | ||||
chr6:95577431-95577553 | Common:3; Rare:33 | ||||
chr6:99425219-99425515 | Common:2; Rare:87 | ||||
chr6:100881272-100881458 | Common:4; Rare:77 | ||||
chr6:106629466-106629661 | Common:3; Rare:46 | ||||
chr6:107958174-107958428 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
chr6:109009384-109009689 | Common:2; Rare:88 | ||||
chr6:109094832-109095043 | Common:2; Rare:60 | ||||
chr6:109095389-109095551 | Rare:35 | ||||
chr6:109382066-109382139 | Common:2; Rare:24 | ||||
chr6:109382209-109382286 | Rare:32 | ||||
chr6:109382332-109382776 | Common:5; Rare:148; Clinvar (benign):2 | ||||
chr6:109455688-109456059 | Common:3; Rare:95 | ||||
chr6:109691158-109691329 | Common:3; Rare:40; Clinvar:4; Clinvar (benign):3 |