Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:83193640-83193747 | Common:1; Rare:44 | ||||
chr11:85628338-85628603 | Common:6; Rare:81 | ||||
chr11:88175439-88175563 | Rare:53 | ||||
chr11:88337720-88337888 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
chr11:93741446-93741695 | Common:5; Rare:102 | ||||
chr11:94493802-94494011 | Common:3; Rare:62; Clinvar (benign):1 | ||||
chr11:94973537-94973699 | Rare:49 | ||||
chr11:95789560-95789884 | Common:3; Rare:144 | ||||
chr11:95790359-95790547 | Rare:76 | ||||
chr11:96389860-96390024 | Common:1; Rare:61 | ||||
chr11:102347111-102347298 | Common:2; Rare:62 | ||||
chr11:102452629-102452894 | Common:1; Rare:85 | ||||
chr11:103092083-103092246 | Common:1; Rare:55 | ||||
chr11:106077326-106077700 | Common:2; Rare:110 | ||||
chr11:107457800-107457951 | Common:2; Rare:44 |