Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:106077326-106077711 | Common:2; Rare:115 | ||||
chr11:107457748-107457957 | Common:3; Rare:68 | ||||
chr11:108009260-108009349 | Rare:45 | ||||
chr11:108121404-108121609 | Common:4; Rare:70; Clinvar:1; Clinvar (benign):4 | ||||
chr11:108222556-108223128 | Common:1; Rare:188; Clinvar:8; Clinvar (benign):1 | ||||
chr11:108223282-108223441 | Rare:44 | ||||
chr11:108467506-108467582 | Rare:24 | ||||
chr11:108664912-108665120 | Common:3; Rare:76 | ||||
chr11:111379173-111379435 | Common:1; Rare:51 | ||||
chr11:111379449-111379478 | Rare:9 | ||||
chr11:111379496-111379524 | Rare:6 | ||||
chr11:111379644-111379974 | Common:2; Rare:55 | ||||
chr11:111602183-111602481 | Common:1; Rare:96 | ||||
chr11:111766348-111766442 | Common:1; Rare:56 | ||||
chr11:111878878-111878945 | Common:2; Rare:13 |