Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:116787970-116788104 | Rare:38 | ||||
chr11:117144197-117144418 | Common:2; Rare:100 | ||||
chr11:117199010-117199430 | Common:6; Rare:132 | ||||
chr11:117232493-117232760 | Common:2; Rare:86 | ||||
chr11:117316255-117316413 | Common:1; Rare:34 | ||||
chr11:117986293-117986447 | Common:3; Rare:60; Clinvar:2 | ||||
chr11:117989878-117990030 | Rare:25 | ||||
chr11:118076818-118077128 | Common:4; Rare:75 | ||||
chr11:118252221-118252384 | Rare:61 | ||||
chr11:118264098-118264654 | Common:2; Rare:111 | ||||
chr11:118344262-118344417 | Common:1; Rare:27; Clinvar:1; Clinvar (benign):1 | ||||
chr11:118401329-118401717 | Rare:132 | ||||
chr11:118572492-118572515 | Rare:10 | ||||
chr11:118790885-118791305 | Rare:142 | ||||
chr11:118910391-118910697 | Common:3; Rare:96 |