Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:114400397-114400761 | Common:2; Rare:138 | ||||
chr11:114439367-114439675 | Common:3; Rare:104 | ||||
chr11:116772965-116773060 | Rare:32 | ||||
chr11:116787991-116788112 | Rare:34 | ||||
chr11:117144205-117144379 | Common:2; Rare:90 | ||||
chr11:117144422-117144591 | Common:9; Rare:57 | ||||
chr11:117198998-117199439 | Common:6; Rare:134 | ||||
chr11:117199468-117199490 | Rare:3 | ||||
chr11:117200001-117200218 | Common:6; Rare:45 | ||||
chr11:117201092-117201389 | Common:3; Rare:58 | ||||
chr11:117201888-117201923 | Rare:5 | ||||
chr11:117232036-117232177 | Rare:36 | ||||
chr11:117232493-117232725 | Common:2; Rare:73 | ||||
chr11:117986327-117986524 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
chr11:117989856-117990030 | Common:1; Rare:27 |