Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:117178602-117178933 | Common:3; Rare:119 | ||||
chr11:117179809-117179890 | Rare:17 | ||||
chr11:117181397-117181628 | Rare:72 | ||||
chr11:117189454-117189772 | Rare:67 | ||||
chr11:117231995-117232309 | Rare:77 | ||||
chr11:117232444-117232663 | Rare:47 | ||||
chr11:117232933-117232982 | Common:1; Rare:13 | ||||
chr11:117327695-117327907 | Common:1; Rare:39 | ||||
chr11:117328031-117328207 | Common:1; Rare:44 | ||||
chr11:117816851-117817026 | Rare:36 | ||||
chr11:117817403-117817580 | Common:5; Rare:32 | ||||
chr11:117817750-117817952 | Common:1; Rare:54 | ||||
chr11:117986057-117986110 | Rare:5 | ||||
chr11:117986211-117986556 | Common:5; Rare:121; Clinvar:6; Clinvar (benign):2 | ||||
chr11:117987094-117987339 | Rare:43 |