Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:111766338-111766426 | Rare:48 | ||||
chr11:111911957-111912118 | Common:3; Rare:33 | ||||
chr11:111912590-111912872 | Common:1; Rare:68 | ||||
chr11:111913138-111913289 | Rare:45 | ||||
chr11:112025339-112025464 | Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
chr11:112074005-112074363 | Common:1; Rare:76 | ||||
chr11:112086729-112086905 | Rare:71; Clinvar:1 | ||||
chr11:112226314-112226461 | Rare:67 | ||||
chr11:113314453-113314594 | Rare:50 | ||||
chr11:113875472-113875762 | Common:4; Rare:103 | ||||
chr11:114400436-114400717 | Common:2; Rare:117 | ||||
chr11:117198994-117199323 | Common:6; Rare:103 | ||||
chr11:117232533-117232725 | Common:2; Rare:66 | ||||
chr11:117986213-117986418 | Common:4; Rare:64; Clinvar:2 | ||||
chr11:118401332-118401678 | Rare:114 |