Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:112226314-112226677 | Common:1; Rare:149; Clinvar:1; Clinvar (pathogenic):3 | ||||
chr11:112961208-112961569 | Common:2; Rare:164 | ||||
chr11:113314386-113314602 | Rare:72 | ||||
chr11:113773668-113773842 | Common:1; Rare:54 | ||||
chr11:113875480-113875815 | Common:4; Rare:124 | ||||
chr11:114400451-114400753 | Common:2; Rare:121 | ||||
chr11:114439293-114439587 | Common:2; Rare:97 | ||||
chr11:115504345-115504673 | Common:2; Rare:107 | ||||
chr11:116772962-116773088 | Rare:44 | ||||
chr11:117144183-117144388 | Common:2; Rare:99 | ||||
chr11:117232036-117232177 | Rare:36 | ||||
chr11:117232517-117232760 | Common:2; Rare:83 | ||||
chr11:117327713-117327949 | Common:2; Rare:41 | ||||
chr11:118359548-118359667 | Common:1; Rare:47 | ||||
chr11:118401320-118401698 | Rare:124 |