Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:111879158-111879541 | Rare:113 | ||||
chr11:112073998-112074349 | Common:1; Rare:72 | ||||
chr11:112086722-112086910 | Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr11:112226316-112226446 | Rare:60 | ||||
chr11:113314444-113314588 | Rare:50 | ||||
chr11:113875503-113875653 | Rare:54 | ||||
chr11:114296266-114296565 | Rare:56 | ||||
chr11:114400421-114400766 | Common:2; Rare:133 | ||||
chr11:116772962-116773069 | Rare:37 | ||||
chr11:116787951-116788095 | Rare:45 | ||||
chr11:117144188-117144418 | Common:2; Rare:105 | ||||
chr11:117232574-117232725 | Common:2; Rare:56 | ||||
chr11:118264221-118264600 | Common:1; Rare:60 | ||||
chr11:118359386-118359659 | Common:3; Rare:109 | ||||
chr11:118401340-118401698 | Rare:120 |