Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:119084796-119084949 | Common:1; Rare:44; Clinvar (benign):1 | ||||
chr11:119101800-119102204 | Rare:102; Clinvar:4 | ||||
chr11:119110630-119110881 | Rare:68 | ||||
chr11:119121219-119121626 | Common:1; Rare:104 | ||||
chr11:119206186-119206396 | Common:5; Rare:91; Clinvar:8; Clinvar (benign):4 | ||||
chr11:119334250-119334544 | Rare:80 | ||||
chr11:119423135-119423374 | Common:3; Rare:65 | ||||
chr11:119729421-119729573 | Rare:40 | ||||
chr11:120325140-120325355 | Common:1; Rare:59 | ||||
chr11:120385214-120385397 | Rare:27 | ||||
chr11:120385819-120385983 | Rare:30 | ||||
chr11:121023864-121024174 | Common:1; Rare:90 | ||||
chr11:121292563-121292923 | Rare:111; Clinvar:3 | ||||
chr11:121452117-121452332 | Common:1; Rare:58 | ||||
chr11:122655579-122655901 | Common:3; Rare:76 |