Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:108222597-108223122 | Common:1; Rare:167; Clinvar:7; Clinvar (benign):1 | ||||
chr11:108223286-108223441 | Rare:44 | ||||
chr11:108467479-108467595 | Rare:43 | ||||
chr11:108593591-108593945 | Common:5; Rare:86 | ||||
chr11:111766338-111766433 | Common:1; Rare:58 | ||||
chr11:111871254-111871334 | Rare:21 | ||||
chr11:111879152-111879551 | Common:1; Rare:121 | ||||
chr11:111912726-111912753 | Rare:4 | ||||
chr11:111913131-111913283 | Rare:44 | ||||
chr11:111977118-111977377 | Common:3; Rare:59 | ||||
chr11:112025339-112025475 | Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
chr11:112073993-112074351 | Common:1; Rare:74 | ||||
chr11:112086725-112086932 | Rare:90; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr11:112164083-112164370 | Common:1; Rare:52 | ||||
chr11:113314403-113314602 | Rare:69 |