Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:117232502-117232736 | Common:2; Rare:75 | ||||
chr11:117316072-117316413 | Common:1; Rare:89 | ||||
chr11:117828024-117828376 | Common:1; Rare:67 | ||||
chr11:117876593-117876785 | Rare:55 | ||||
chr11:117986254-117986507 | Common:5; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
chr11:117989731-117990073 | Common:1; Rare:50 | ||||
chr11:118145420-118145555 | Rare:37 | ||||
chr11:118252282-118252497 | Rare:55 | ||||
chr11:118264284-118264593 | Common:1; Rare:50 | ||||
chr11:118342603-118342834 | Common:2; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
chr11:118344258-118344417 | Common:1; Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
chr11:118359410-118359667 | Common:3; Rare:105 | ||||
chr11:118401341-118401724 | Rare:128 | ||||
chr11:118572331-118572494 | Common:2; Rare:59 | ||||
chr11:118621176-118621529 | Rare:73 |