Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:106325551-106325906 | Common:1; Rare:118 | ||||
chr6:106629467-106629640 | Common:3; Rare:38 | ||||
chr6:107958088-107958428 | Common:1; Rare:104; Clinvar:2; Clinvar (benign):2 | ||||
chr6:108260918-108261102 | Rare:87 | ||||
chr6:108294765-108295070 | Common:1; Rare:81 | ||||
chr6:109382209-109382308 | Rare:43 | ||||
chr6:109455702-109456018 | Common:2; Rare:87 | ||||
chr6:109483137-109483236 | Rare:47 | ||||
chr6:109691145-109691322 | Common:3; Rare:46; Clinvar:4; Clinvar (benign):3 | ||||
chr6:110179917-110180142 | Common:2; Rare:65 | ||||
chr6:110958539-110958788 | Common:6; Rare:85 | ||||
chr6:111483642-111483775 | Common:1; Rare:50 | ||||
chr6:112087421-112087691 | Rare:88 | ||||
chr6:116254019-116254173 | Common:2; Rare:45 | ||||
chr6:116279307-116279469 | Common:1; Rare:67 |