Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:108222597-108222787 | Rare:63 | ||||
chr11:108664918-108665106 | Common:3; Rare:67 | ||||
chr11:111602177-111602472 | Common:1; Rare:96 | ||||
chr11:111766363-111766433 | Common:1; Rare:39 | ||||
chr11:111878837-111878950 | Common:2; Rare:30 | ||||
chr11:111879427-111879539 | Rare:37 | ||||
chr11:112074011-112074356 | Common:1; Rare:70 | ||||
chr11:112086716-112086932 | Rare:96; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr11:113875497-113875818 | Common:4; Rare:123 | ||||
chr11:114400456-114400738 | Common:2; Rare:117 | ||||
chr11:116772965-116773066 | Rare:34 | ||||
chr11:117144188-117144350 | Common:2; Rare:82 | ||||
chr11:118264252-118264418 | Rare:28 | ||||
chr11:118401320-118401668 | Rare:113 | ||||
chr11:118790919-118791219 | Rare:81 |