Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:95923829-95924157 | Common:2; Rare:145; Clinvar:5; Clinvar (benign):5 | ||||
chr11:96389854-96390052 | Common:1; Rare:82 | ||||
chr11:102110201-102110460 | Rare:100 | ||||
chr11:102317364-102317563 | Rare:49 | ||||
chr11:102347111-102347313 | Common:2; Rare:67 | ||||
chr11:102451840-102452125 | Rare:73 | ||||
chr11:102452288-102452442 | Common:2; Rare:35 | ||||
chr11:102452523-102452900 | Common:1; Rare:127 | ||||
chr11:103092028-103092217 | Common:1; Rare:57 | ||||
chr11:106077317-106077734 | Common:2; Rare:133 | ||||
chr11:108009225-108009363 | Rare:61 | ||||
chr11:108121378-108121707 | Common:6; Rare:108; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr11:108134152-108134316 | Common:1; Rare:41; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr11:108222597-108223128 | Common:1; Rare:168; Clinvar:8; Clinvar (benign):1 | ||||
chr11:108223308-108223435 | Rare:37 |